Linked Data
ClinVar Variation Id:
3032058
ClinVar RCV Id:
RCV004534546
dbSNP Id:
rs1418352110
gnomAD v3:
7-117479908-G-T
gnomAD v4:
7-117479908-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117479908G>T , CM000669.2:g.117479908G>T | GRCh38 |
| NC_000007.13:g.117119962G>T , CM000669.1:g.117119962G>T | GRCh37 |
| NC_000007.12:g.116907198G>T | NCBI36 |
| NG_016465.4:g.19125G>T , LRG_663:g.19125G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000446805.2:c.-191+214G>T | ENSP00000417012.1:n.-191+214G>T | |
| ENST00000673785.1:c.-406+14077G>T | ENSP00000501235.1:n.-406+14077G>T | |
| ENST00000446805.1:c.-191+214G>T | ENSP00000417012.1:n.-191+214G>T | |
| ENST00000546407.1:n.166+4100G>T | ||
| XM_011515751.1:c.143+563G>T | XP_011514053.1:n.143+563G>T | |
| XM_011515752.1:c.143+563G>T | XP_011514054.1:n.143+563G>T | |
| XM_011515753.1:c.-191+214G>T | XP_011514055.1:n.-191+214G>T | |
| XM_011515754.1:c.-519+214G>T | XP_011514056.1:n.-519+214G>T |