Linked Data
ClinVar Variation Id:
217154
dbSNP Id:
rs863224961
gnomAD v2:
15-42701579-G-T
gnomAD v4:
15-42409381-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42409381G>T , CM000677.2:g.42409381G>T | GRCh38 |
| NC_000015.9:g.42701579G>T , CM000677.1:g.42701579G>T | GRCh37 |
| NC_000015.8:g.40488871G>T | NCBI36 |
| NG_008660.1:g.66279G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000337571.9:c.-4+1G>T | ENSP00000336840.4:n.-4+1G>T | |
| ENST00000349748.8:c.1716+1G>T | ENSP00000183936.4:n.1716+1G>T | |
| ENST00000357568.8:c.1974+1G>T | ENSP00000350181.3:n.1974+1G>T | |
| ENST00000397163.8:c.1992+1G>T MANE Select | ENSP00000380349.3:n.1992+1G>T | |
| ENST00000397204.9:c.-4+1G>T | ENSP00000380387.4:n.-4+1G>T | |
| ENST00000466222.7:n.257+1G>T | ||
| ENST00000466369.5:n.2483+1G>T | ||
| ENST00000495723.1:n.2863+1G>T | ||
| ENST00000549793.5:n.2205+1G>T | ||
| ENST00000569136.6:c.-4+1G>T | ENSP00000455254.1:n.-4+1G>T | |
| ENST00000638141.2:n.1731+1G>T | ||
| ENST00000673646.1:c.556+1G>T | ENSP00000501007.1:n.556+1G>T | |
| ENST00000673687.1:n.69+1G>T | ||
| ENST00000673692.1:c.-3-406G>T | ENSP00000501138.1:n.-3-406G>T | |
| ENST00000673705.1:c.387+1G>T | ENSP00000501021.1:n.387+1G>T | |
| ENST00000673743.1:c.-101+1G>T | ENSP00000500989.1:n.-101+1G>T | |
| ENST00000673750.1:c.-4+1G>T | ENSP00000501173.1:n.-4+1G>T | |
| ENST00000673771.1:c.-4+1G>T | ENSP00000501023.1:n.-4+1G>T | |
| ENST00000673774.1:n.288G>T | ||
| ENST00000673839.1:c.-148+1G>T | ENSP00000501188.1:n.-148+1G>T | |
| ENST00000673851.1:c.-4+1G>T | ENSP00000501142.1:n.-4+1G>T | |
| ENST00000673854.1:n.5414+1G>T | ||
| ENST00000673886.1:c.-4+1G>T | ENSP00000501155.1:n.-4+1G>T | |
| ENST00000673890.1:c.-4+1G>T | ENSP00000501293.1:n.-4+1G>T | |
| ENST00000673928.1:c.-4+1G>T | ENSP00000501099.1:n.-4+1G>T | |
| ENST00000673936.1:c.-4+1G>T | ENSP00000501189.1:n.-4+1G>T | |
| ENST00000673939.1:c.-4+1G>T | ENSP00000501129.1:n.-4+1G>T | |
| ENST00000673950.1:n.266+1G>T | ||
| ENST00000673978.1:c.135+1G>T | ENSP00000500976.1:n.135+1G>T | |
| ENST00000673987.1:c.-4+1G>T | ENSP00000501231.1:n.-4+1G>T | |
| ENST00000674011.1:c.-4+1G>T | ENSP00000501171.1:n.-4+1G>T | |
| ENST00000674018.1:c.-4+1G>T | ENSP00000501271.1:n.-4+1G>T | |
| ENST00000674027.1:n.52+1G>T | ||
| ENST00000674041.1:c.-4+1G>T | ENSP00000500956.1:n.-4+1G>T | |
| ENST00000674052.1:c.216+1G>T | ENSP00000501057.1:n.216+1G>T | |
| ENST00000674093.1:c.-4+1G>T | ENSP00000501303.1:n.-4+1G>T | |
| ENST00000674119.1:c.-4+1G>T | ENSP00000501217.1:n.-4+1G>T | |
| ENST00000674135.1:c.174+1G>T | ENSP00000501178.1:n.174+1G>T | |
| ENST00000674139.1:c.-4+1G>T | ENSP00000501054.1:n.-4+1G>T | |
| ENST00000674146.1:c.-4+1G>T | ENSP00000501175.1:n.-4+1G>T | |
| ENST00000674149.1:c.-4+1G>T | ENSP00000501112.1:n.-4+1G>T | |
| ENST00000318023.11:c.1848+1G>T | ENSP00000326281.8:n.1848+1G>T | |
| ENST00000337571.8:c.-4+1G>T | ENSP00000336840.4:n.-4+1G>T | |
| ENST00000349748.7:c.1716+1G>T | ENSP00000183936.4:n.1716+1G>T | |
| ENST00000356316.7:c.-4+1G>T | ENSP00000348667.4:n.-4+1G>T | |
| ENST00000357568.7:c.1974+1G>T | ENSP00000350181.3:n.1974+1G>T | |
| ENST00000397163.7:c.1992+1G>T | ENSP00000380349.3:n.1992+1G>T | |
| ENST00000397200.8:c.456+1G>T | ENSP00000380384.4:n.456+1G>T | |
| ENST00000397204.8:c.-4+1G>T | ENSP00000380387.4:n.-4+1G>T | |
| ENST00000466222.6:n.915+1G>T | ||
| ENST00000561817.5:c.-4+1G>T | ENSP00000456575.1:n.-4+1G>T | |
| ENST00000564503.5:c.89+1G>T | ||
| ENST00000565274.5:c.204+1G>T | ENSP00000457759.1:n.204+1G>T | |
| ENST00000565559.5:c.174+1G>T | ENSP00000457878.1:n.174+1G>T | |
| ENST00000567071.5:c.472+1G>T | ||
| ENST00000569136.5:c.-4+1G>T | ENSP00000455254.1:n.-4+1G>T | |
| ENST00000569827.5:c.324+1G>T | ENSP00000454379.1:n.324+1G>T | |
| NM_000070.2:c.1992+1G>T | NP_000061.1:n.1992+1G>T | |
| NM_024344.1:c.1974+1G>T | NP_077320.1:n.1974+1G>T | |
| NM_173087.1:c.1716+1G>T | NP_775110.1:n.1716+1G>T | |
| NM_173088.1:c.456+1G>T | NP_775111.1:n.456+1G>T | |
| NM_173089.1:c.-4+1G>T | NP_775112.1:n.-4+1G>T | |
| NM_173090.1:c.-4+1G>T | NP_775113.1:n.-4+1G>T | |
| NM_000070.3:c.1992+1G>T MANE Select | NP_000061.1:n.1992+1G>T | |
| NM_024344.2:c.1974+1G>T | NP_077320.1:n.1974+1G>T | |
| NM_173087.2:c.1716+1G>T | NP_775110.1:n.1716+1G>T | |
| NM_173088.2:c.456+1G>T | NP_775111.1:n.456+1G>T | |
| NM_173089.2:c.-4+1G>T | NP_775112.1:n.-4+1G>T | |
| NM_173090.2:c.-4+1G>T | NP_775113.1:n.-4+1G>T |