Linked Data
ClinVar Variation Id:
98899
ClinVar RCV Id:
RCV000085232
RCV000668398
RCV001003189
RCV001074560
RCV001250674
RCV002498451
RCV003460771
dbSNP Id:
rs61751279
ExAC:
1:68912545 T / A
gnomAD v2:
1-68912545-T-A
gnomAD v3:
1-68446862-T-A
gnomAD v4:
1-68446862-T-A
ERepo:
CA226591/MONDO:0100368/120
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68446862T>A , CM000663.2:g.68446862T>A | GRCh38 |
| NC_000001.10:g.68912545T>A , CM000663.1:g.68912545T>A | GRCh37 |
| NC_000001.9:g.68685133T>A | NCBI36 |
| NG_008472.1:g.8098A>T | |
| NG_008472.2:g.8098A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.95-2A>T MANE Select | ENSP00000262340.5:n.95-2A>T | |
| ENST00000262340.5:c.95-2A>T | ENSP00000262340.5:n.95-2A>T | |
| NM_000329.2:c.95-2A>T | NP_000320.1:n.95-2A>T | |
| XM_017002027.1:c.-32+1762A>T | XP_016857516.1:n.-32+1762A>T | |
| NM_000329.3:c.95-2A>T MANE Select | NP_000320.1:n.95-2A>T |