Linked Data
gnomAD v4:
7-107710128-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107710128G>A , CM000669.2:g.107710128G>A | GRCh38 |
| NC_000007.13:g.107350573G>A , CM000669.1:g.107350573G>A | GRCh37 |
| NC_000007.12:g.107137809G>A | NCBI36 |
| NG_008489.1:g.54494G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644269.2:c.2164G>A MANE Select | ENSP00000494017.1:p.Val722Ile | |
| ENST00000644846.1:c.820G>A | ||
| ENST00000265715.7:c.2164G>A | ENSP00000265715.3:p.Val722Ile | |
| ENST00000492030.2:n.377-27G>A | ||
| NM_000441.1:c.2164G>A | NP_000432.1:p.Val722Ile | |
| XM_005250425.1:c.2164G>A | XP_005250482.1:p.Val722Ile | |
| XM_005250425.2:c.2164G>A | XP_005250482.1:p.Val722Ile | |
| XM_017012318.1:c.2086G>A | XP_016867807.1:p.Val696Ile | |
| NM_000441.2:c.2164G>A MANE Select | NP_000432.1:p.Val722Ile |