Linked Data
ClinVar Variation Id:
766535
ClinVar RCV Id:
RCV001427469
dbSNP Id:
rs1587668828
gnomAD v4:
9-92719076-G-A
MyVariant Identifiers:
chr9:g.95481358G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.92719076G>A , CM000671.2:g.92719076G>A | GRCh38 |
| NC_000009.11:g.95481358G>A , CM000671.1:g.95481358G>A | GRCh37 |
| NC_000009.10:g.94521179G>A | NCBI36 |
| NG_033908.1:g.50726C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356884.11:c.1569C>T MANE Select | ENSP00000349351.6:p.Ala523= | |
| ENST00000356884.10:c.1569C>T | ENSP00000349351.6:p.Ala523= | |
| ENST00000375512.3:c.1569C>T | ENSP00000364662.3:p.Ala523= | |
| NM_001003800.1:c.1569C>T | NP_001003800.1:p.Ala523= | |
| NM_015250.3:c.1569C>T | NP_056065.1:p.Ala523= | |
| XM_017014551.1:c.1650C>T | XP_016870040.1:p.Ala550= | |
| NM_001003800.2:c.1569C>T MANE Select | NP_001003800.1:p.Ala523= | |
| NM_015250.4:c.1569C>T | NP_056065.1:p.Ala523= |