Linked Data
gnomAD v4:
7-117479616-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117479616T>C , CM000669.2:g.117479616T>C | GRCh38 |
| NC_000007.13:g.117119670T>C , CM000669.1:g.117119670T>C | GRCh37 |
| NC_000007.12:g.116906906T>C | NCBI36 |
| NG_016465.4:g.18833T>C , LRG_663:g.18833T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446805.2:c.-269T>C | ENSP00000417012.1:n.-269T>C | |
| ENST00000673785.1:c.-406+13785T>C | ENSP00000501235.1:n.-406+13785T>C | |
| ENST00000446805.1:c.-269T>C | ENSP00000417012.1:n.-269T>C | |
| ENST00000546407.1:n.166+3808T>C | ||
| XM_011515751.1:c.143+271T>C | XP_011514053.1:n.143+271T>C | |
| XM_011515752.1:c.143+271T>C | XP_011514054.1:n.143+271T>C | |
| XM_011515753.1:c.-269T>C | XP_011514055.1:n.-269T>C | |
| XM_011515754.1:c.-597T>C | XP_011514056.1:n.-597T>C |