Linked Data
ClinVar Variation Id:
470668
ClinVar RCV Id:
RCV000526021
dbSNP Id:
rs548860628
ExAC:
15:73615029 G / A
gnomAD v2:
15-73615029-G-A
gnomAD v3:
15-73322688-G-A
gnomAD v4:
15-73322688-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322688G>A , CM000677.2:g.73322688G>A | GRCh38 |
| NC_000015.9:g.73615029G>A , CM000677.1:g.73615029G>A | GRCh37 |
| NC_000015.8:g.71402082G>A | NCBI36 |
| NG_009063.1:g.51577C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000261917.4:c.3405C>T MANE Select | ENSP00000261917.3:p.Leu1135= | |
| ENST00000261917.3:c.3405C>T | ENSP00000261917.3:p.Leu1135= | |
| NM_005477.2:c.3405C>T | NP_005468.1:p.Leu1135= | |
| XM_011521148.1:c.2187C>T | XP_011519450.1:p.Leu729= | |
| XM_011521148.2:c.2187C>T | XP_011519450.1:p.Leu729= | |
| NM_005477.3:c.3405C>T MANE Select | NP_005468.1:p.Leu1135= |