Linked Data
ClinVar Variation Id:
1479499
ClinVar RCV Id:
RCV001990960
dbSNP Id:
rs778126810
ExAC:
19:17940920 A / T
gnomAD v2:
19-17940920-A-T
gnomAD v3:
19-17830111-A-T
gnomAD v4:
19-17830111-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.17830111A>T , CM000681.2:g.17830111A>T | GRCh38 |
| NC_000019.9:g.17940920A>T , CM000681.1:g.17940920A>T | GRCh37 |
| NC_000019.8:g.17801920A>T | NCBI36 |
| NG_007273.1:g.22881T>A , LRG_77:g.22881T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000526008.6:c.*1761T>A | ENSP00000513006.1:n.*1761T>A | |
| ENST00000696967.1:n.2381T>A | ||
| ENST00000696968.1:n.437T>A | ||
| ENST00000696969.1:n.2161T>A | ||
| ENST00000458235.7:c.3204T>A MANE Select | ENSP00000391676.1:p.Ala1068= | |
| ENST00000458235.5:c.3204T>A | ENSP00000391676.1:p.Ala1068= | |
| ENST00000527031.5:n.2279-4801T>A | ||
| ENST00000527670.5:c.3204T>A | ENSP00000432511.1:p.Ala1068= | |
| ENST00000534444.1:c.3204T>A | ENSP00000436421.1:p.Ala1068= | |
| NM_000215.3:c.3204T>A , LRG_77t1:c.3204T>A | NP_000206.2:p.Ala1068= | |
| XM_005259896.2:c.3333T>A | XP_005259953.1:p.Ala1111= | |
| XM_006722745.2:c.3204T>A | XP_006722808.1:p.Ala1068= | |
| XM_005259896.3:c.3333T>A | XP_005259953.1:p.Ala1111= | |
| NM_000215.4:c.3204T>A MANE Select | NP_000206.2:p.Ala1068= |