Linked Data
ClinVar Variation Id:
1665839
ClinVar RCV Id:
RCV002203298
dbSNP Id:
rs145440508
ExAC:
10:73767413 G / A
gnomAD v2:
10-73767413-G-A
gnomAD v3:
10-72007655-G-A
gnomAD v4:
10-72007655-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.72007655G>A , CM000672.2:g.72007655G>A | GRCh38 |
| NC_000010.10:g.73767413G>A , CM000672.1:g.73767413G>A | GRCh37 |
| NC_000010.9:g.73437419G>A | NCBI36 |
| NG_012635.1:g.48294G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373115.5:c.624G>A MANE Select | ENSP00000362207.4:p.Thr208= | |
| ENST00000373115.4:c.624G>A | ENSP00000362207.4:p.Thr208= | |
| NM_004273.4:c.624G>A | NP_004264.2:p.Thr208= | |
| XM_006718075.2:c.624G>A | XP_006718138.1:p.Thr208= | |
| XM_011540369.1:c.624G>A | XP_011538671.1:p.Thr208= | |
| XM_006718075.4:c.624G>A | XP_006718138.1:p.Thr208= | |
| XM_011540369.2:c.624G>A | XP_011538671.1:p.Thr208= | |
| NM_004273.5:c.624G>A MANE Select | NP_004264.2:p.Thr208= |