Linked Data
ClinVar Variation Id:
2700345
ClinVar RCV Id:
RCV003517952
dbSNP Id:
rs894156945
gnomAD v4:
15-42402964-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.42402964C>T , CM000677.2:g.42402964C>T | GRCh38 |
| NC_000015.9:g.42695162C>T , CM000677.1:g.42695162C>T | GRCh37 |
| NC_000015.8:g.40482454C>T | NCBI36 |
| NG_008660.1:g.59862C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000349748.8:c.1563C>T | ENSP00000183936.4:p.Phe521= | |
| ENST00000357568.8:c.1707C>T | ENSP00000350181.3:p.Phe569= | |
| ENST00000397163.8:c.1707C>T MANE Select | ENSP00000380349.3:p.Phe569= | |
| ENST00000466369.5:n.2216C>T | ||
| ENST00000483208.5:n.2596C>T | ||
| ENST00000495723.1:n.2596C>T | ||
| ENST00000549793.5:n.1938C>T | ||
| ENST00000638141.2:n.1578C>T | ||
| ENST00000673646.1:c.171C>T | ENSP00000501007.1:p.Phe57= | |
| ENST00000673705.1:c.309+3312C>T | ENSP00000501021.1:n.309+3312C>T | |
| ENST00000673813.1:n.580+49C>T | ||
| ENST00000318023.11:c.1563C>T | ENSP00000326281.8:p.Phe521= | |
| ENST00000349748.7:c.1563C>T | ENSP00000183936.4:p.Phe521= | |
| ENST00000357568.7:c.1707C>T | ENSP00000350181.3:p.Phe569= | |
| ENST00000397163.7:c.1707C>T | ENSP00000380349.3:p.Phe569= | |
| ENST00000397200.8:c.171C>T | ENSP00000380384.4:p.Phe57= | |
| ENST00000567071.5:c.166C>T | ||
| ENST00000569827.5:c.171C>T | ENSP00000454379.1:p.Phe57= | |
| NM_000070.2:c.1707C>T | NP_000061.1:p.Phe569= | |
| NM_024344.1:c.1707C>T | NP_077320.1:p.Phe569= | |
| NM_173087.1:c.1563C>T | NP_775110.1:p.Phe521= | |
| NM_173088.1:c.171C>T | NP_775111.1:p.Phe57= | |
| NM_000070.3:c.1707C>T MANE Select | NP_000061.1:p.Phe569= | |
| NM_024344.2:c.1707C>T | NP_077320.1:p.Phe569= | |
| NM_173087.2:c.1563C>T | NP_775110.1:p.Phe521= | |
| NM_173088.2:c.171C>T | NP_775111.1:p.Phe57= |