Linked Data
ClinVar Variation Id:
281184
dbSNP Id:
rs886042108
gnomAD v4:
15-42409930-G-T
PubMed:
PMID:23891399
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42409930G>T , CM000677.2:g.42409930G>T | GRCh38 |
| NC_000015.9:g.42702128G>T , CM000677.1:g.42702128G>T | GRCh37 |
| NC_000015.8:g.40489420G>T | NCBI36 |
| NG_008660.1:g.66828G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337571.9:c.56-1G>T | ENSP00000336840.4:n.56-1G>T | |
| ENST00000349748.8:c.1775-1G>T | ENSP00000183936.4:n.1775-1G>T | |
| ENST00000357568.8:c.2033-1G>T | ENSP00000350181.3:n.2033-1G>T | |
| ENST00000397163.8:c.2051-1G>T MANE Select | ENSP00000380349.3:n.2051-1G>T | |
| ENST00000397204.9:c.56-1G>T | ENSP00000380387.4:n.56-1G>T | |
| ENST00000466222.7:n.316-1G>T | ||
| ENST00000466369.5:n.2542-1G>T | ||
| ENST00000495723.1:n.2922-1G>T | ||
| ENST00000549793.5:n.2264-1G>T | ||
| ENST00000562199.2:c.59-1G>T | ENSP00000501034.1:n.59-1G>T | |
| ENST00000569136.6:c.56-1G>T | ENSP00000455254.1:n.56-1G>T | |
| ENST00000638141.2:n.1790-1G>T | ||
| ENST00000673646.1:c.615-1G>T | ENSP00000501007.1:n.615-1G>T | |
| ENST00000673687.1:n.128-1G>T | ||
| ENST00000673692.1:c.56-1G>T | ENSP00000501138.1:n.56-1G>T | |
| ENST00000673705.1:c.446-1G>T | ENSP00000501021.1:n.446-1G>T | |
| ENST00000673743.1:c.-42-6G>T | ENSP00000500989.1:n.-42-6G>T | |
| ENST00000673750.1:c.56-1G>T | ENSP00000501173.1:n.56-1G>T | |
| ENST00000673771.1:c.56-1G>T | ENSP00000501023.1:n.56-1G>T | |
| ENST00000673774.1:n.752-1G>T | ||
| ENST00000673839.1:c.56-1G>T | ENSP00000501188.1:n.56-1G>T | |
| ENST00000673851.1:c.56-1G>T | ENSP00000501142.1:n.56-1G>T | |
| ENST00000673854.1:n.5473-1G>T | ||
| ENST00000673886.1:c.56-1G>T | ENSP00000501155.1:n.56-1G>T | |
| ENST00000673890.1:c.56-1G>T | ENSP00000501293.1:n.56-1G>T | |
| ENST00000673928.1:c.56-1G>T | ENSP00000501099.1:n.56-1G>T | |
| ENST00000673936.1:c.56-1G>T | ENSP00000501189.1:n.56-1G>T | |
| ENST00000673939.1:c.56-1G>T | ENSP00000501129.1:n.56-1G>T | |
| ENST00000673950.1:n.325-1G>T | ||
| ENST00000673978.1:c.194-1G>T | ENSP00000500976.1:n.194-1G>T | |
| ENST00000673987.1:c.56-1G>T | ENSP00000501231.1:n.56-1G>T | |
| ENST00000674011.1:c.56-1G>T | ENSP00000501171.1:n.56-1G>T | |
| ENST00000674018.1:c.56-1G>T | ENSP00000501271.1:n.56-1G>T | |
| ENST00000674027.1:n.111-1G>T | ||
| ENST00000674041.1:c.56-1G>T | ENSP00000500956.1:n.56-1G>T | |
| ENST00000674052.1:c.275-1G>T | ENSP00000501057.1:n.275-1G>T | |
| ENST00000674093.1:c.56-1G>T | ENSP00000501303.1:n.56-1G>T | |
| ENST00000674119.1:c.56-1G>T | ENSP00000501217.1:n.56-1G>T | |
| ENST00000674130.1:n.269-1G>T | ||
| ENST00000674135.1:c.233-1G>T | ENSP00000501178.1:n.233-1G>T | |
| ENST00000674139.1:c.56-1G>T | ENSP00000501054.1:n.56-1G>T | |
| ENST00000674146.1:c.56-1G>T | ENSP00000501175.1:n.56-1G>T | |
| ENST00000674149.1:c.56-1G>T | ENSP00000501112.1:n.56-1G>T | |
| ENST00000318023.11:c.1907-1G>T | ENSP00000326281.8:n.1907-1G>T | |
| ENST00000337571.8:c.56-1G>T | ENSP00000336840.4:n.56-1G>T | |
| ENST00000349748.7:c.1775-1G>T | ENSP00000183936.4:n.1775-1G>T | |
| ENST00000356316.7:c.56-1G>T | ENSP00000348667.4:n.56-1G>T | |
| ENST00000357568.7:c.2033-1G>T | ENSP00000350181.3:n.2033-1G>T | |
| ENST00000397163.7:c.2051-1G>T | ENSP00000380349.3:n.2051-1G>T | |
| ENST00000397200.8:c.515-1G>T | ENSP00000380384.4:n.515-1G>T | |
| ENST00000397204.8:c.56-1G>T | ENSP00000380387.4:n.56-1G>T | |
| ENST00000466222.6:n.974-1G>T | ||
| ENST00000561817.5:c.56-1G>T | ENSP00000456575.1:n.56-1G>T | |
| ENST00000562199.1:n.59-1G>T | ||
| ENST00000564503.5:c.148-1G>T | ||
| ENST00000565274.5:c.263-1G>T | ENSP00000457759.1:n.263-1G>T | |
| ENST00000565559.5:c.233-1G>T | ENSP00000457878.1:n.233-1G>T | |
| ENST00000567071.5:c.531-1G>T | ||
| ENST00000569136.5:c.56-1G>T | ENSP00000455254.1:n.56-1G>T | |
| ENST00000569827.5:c.383-1G>T | ENSP00000454379.1:n.383-1G>T | |
| NM_000070.2:c.2051-1G>T | NP_000061.1:n.2051-1G>T | |
| NM_024344.1:c.2033-1G>T | NP_077320.1:n.2033-1G>T | |
| NM_173087.1:c.1775-1G>T | NP_775110.1:n.1775-1G>T | |
| NM_173088.1:c.515-1G>T | NP_775111.1:n.515-1G>T | |
| NM_173089.1:c.56-1G>T | NP_775112.1:n.56-1G>T | |
| NM_173090.1:c.56-1G>T | NP_775113.1:n.56-1G>T | |
| NM_000070.3:c.2051-1G>T MANE Select | NP_000061.1:n.2051-1G>T | |
| NM_024344.2:c.2033-1G>T | NP_077320.1:n.2033-1G>T | |
| NM_173087.2:c.1775-1G>T | NP_775110.1:n.1775-1G>T | |
| NM_173088.2:c.515-1G>T | NP_775111.1:n.515-1G>T | |
| NM_173089.2:c.56-1G>T | NP_775112.1:n.56-1G>T | |
| NM_173090.2:c.56-1G>T | NP_775113.1:n.56-1G>T |