Linked Data
ClinVar Variation Id:
362546
dbSNP Id:
rs77253713
ExAC:
8:22019251 C / T
gnomAD v2:
8-22019251-C-T
gnomAD v3:
8-22161738-C-T
gnomAD v4:
8-22161738-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.22161738C>T , CM000670.2:g.22161738C>T | GRCh38 |
| NC_000008.10:g.22019251C>T , CM000670.1:g.22019251C>T | GRCh37 |
| NC_000008.9:g.22075196C>T | NCBI36 |
| NG_016968.1:g.5068C>T | |
| NG_029659.1:g.1599C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000318561.7:c.-91C>T | ENSP00000316152.3:n.-91C>T | |
| ENST00000524318.3:n.740-38C>T | ||
| NM_001172357.1:c.-91C>T | NP_001165828.1:n.-91C>T | |
| NM_001172410.1:c.-91C>T | NP_001165881.1:n.-91C>T | |
| NM_003018.3:c.-91C>T | NP_003009.2:n.-91C>T | |
| XM_011544612.1:c.-91C>T | XP_011542914.1:n.-91C>T | |
| XM_011544613.1:c.-91C>T | XP_011542915.1:n.-91C>T | |
| NM_001317778.1:c.-91C>T | NP_001304707.1:n.-91C>T | |
| NM_001317779.1:c.-91C>T | NP_001304708.1:n.-91C>T | |
| NM_001317780.1:c.-91C>T | NP_001304709.1:n.-91C>T | |
| XM_011544613.3:c.-91C>T | XP_011542915.1:n.-91C>T | |
| NM_001385654.1:c.-53-38C>T | NP_001372583.1:n.-53-38C>T | |
| NM_001385655.1:c.-53-38C>T | NP_001372584.1:n.-53-38C>T | |
| NM_001385656.1:c.-53-38C>T | NP_001372585.1:n.-53-38C>T | |
| NM_001385657.1:c.-53-38C>T | NP_001372586.1:n.-53-38C>T | |
| NM_001385658.1:c.-53-38C>T | NP_001372587.1:n.-53-38C>T | |
| NM_001385659.1:c.-53-38C>T | NP_001372588.1:n.-53-38C>T | |
| NM_001385660.1:c.-53-38C>T | NP_001372589.1:n.-53-38C>T |