Linked Data
dbSNP Id:
rs1664022802
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29227074A>T , CM000664.2:g.29227074A>T | GRCh38 |
| NC_000002.11:g.29449940A>T , CM000664.1:g.29449940A>T | GRCh37 |
| NC_000002.10:g.29303444A>T | NCBI36 |
| NG_009445.1:g.699493T>A , LRG_488:g.699493T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389048.8:c.2915T>A MANE Select | ENSP00000373700.3:p.Val972Glu | |
| ENST00000431873.6:c.81T>A | ||
| ENST00000389048.7:c.2915T>A | ENSP00000373700.3:p.Val972Glu | |
| ENST00000618119.4:c.1784T>A | ENSP00000482733.1:p.Val595Glu | |
| NM_004304.4:c.2915T>A | NP_004295.2:p.Val972Glu | |
| XM_024452778.1:c.68T>A | XP_024308546.1:p.Val23Glu | |
| XR_001738688.2:n.3771T>A | ||
| NM_004304.5:c.2915T>A MANE Select | NP_004295.2:p.Val972Glu |