Linked Data
gnomAD v4:
7-117479569-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117479569T>A , CM000669.2:g.117479569T>A | GRCh38 |
| NC_000007.13:g.117119623T>A , CM000669.1:g.117119623T>A | GRCh37 |
| NC_000007.12:g.116906859T>A | NCBI36 |
| NG_016465.4:g.18786T>A , LRG_663:g.18786T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446805.2:c.-316T>A | ENSP00000417012.1:n.-316T>A | |
| ENST00000673785.1:c.-406+13738T>A | ENSP00000501235.1:n.-406+13738T>A | |
| ENST00000446805.1:c.-316T>A | ENSP00000417012.1:n.-316T>A | |
| ENST00000546407.1:n.166+3761T>A | ||
| XM_011515751.1:c.143+224T>A | XP_011514053.1:n.143+224T>A | |
| XM_011515752.1:c.143+224T>A | XP_011514054.1:n.143+224T>A | |
| XM_011515753.1:c.-316T>A | XP_011514055.1:n.-316T>A | |
| XM_011515754.1:c.-644T>A | XP_011514056.1:n.-644T>A |