Linked Data
gnomAD v4:
7-117479820-G-GC
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117479821dup , CM000669.2:g.117479821dup | GRCh38 |
| NC_000007.13:g.117119875dup , CM000669.1:g.117119875dup | GRCh37 |
| NC_000007.12:g.116907111dup | NCBI36 |
| NG_016465.4:g.19038dup , LRG_663:g.19038dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446805.2:c.-191+127dup | ENSP00000417012.1:n.-191+127dup | |
| ENST00000673785.1:c.-406+13990dup | ENSP00000501235.1:n.-406+13990dup | |
| ENST00000446805.1:c.-191+127dup | ENSP00000417012.1:n.-191+127dup | |
| ENST00000546407.1:n.166+4013dup | ||
| XM_011515751.1:c.143+476dup | XP_011514053.1:n.143+476dup | |
| XM_011515752.1:c.143+476dup | XP_011514054.1:n.143+476dup | |
| XM_011515753.1:c.-191+127dup | XP_011514055.1:n.-191+127dup | |
| XM_011515754.1:c.-519+127dup | XP_011514056.1:n.-519+127dup |