Linked Data
ClinVar Variation Id:
451
ClinVar RCV Id:
RCV000000480
dbSNP Id:
rs121917866
gnomAD v2:
3-98304466-G-A
gnomAD v4:
3-98585622-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.98585622G>A , CM000665.2:g.98585622G>A | GRCh38 |
| NC_000003.11:g.98304466G>A , CM000665.1:g.98304466G>A | GRCh37 |
| NC_000003.10:g.99787156G>A | NCBI36 |
| NG_015994.1:g.12990C>T | |
| NG_015994.2:g.12990C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647941.2:c.991C>T MANE Select | ENSP00000497326.1:p.Arg331Trp | |
| ENST00000264193.2:c.991C>T | ENSP00000264193.2:p.Arg331Trp | |
| ENST00000510489.1:n.241C>T | ||
| NM_000097.5:c.991C>T | NP_000088.3:p.Arg331Trp | |
| XM_005247125.3:c.991C>T | XP_005247182.1:p.Arg331Trp | |
| NM_000097.7:c.991C>T MANE Select | NP_000088.3:p.Arg331Trp | |
| XM_005247125.4:c.991C>T | XP_005247182.1:p.Arg331Trp | |
| XR_001740025.2:n.1162C>T | ||
| XR_001740026.1:n.1726C>T | ||
| XR_001740027.1:n.1266C>T | ||
| XR_001740028.1:n.1232C>T |