Linked Data
ClinVar Variation Id:
2544777
ClinVar RCV Id:
RCV003257187
dbSNP Id:
rs2083970247
gnomAD v4:
22-19176923-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.19176923G>A , CM000684.2:g.19176923G>A | GRCh38 |
| NC_000022.10:g.19164436G>A , CM000684.1:g.19164436G>A | GRCh37 |
| NC_000022.9:g.17544436G>A | NCBI36 |
| NG_033863.1:g.6941C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000215882.10:c.554C>T MANE Select | ENSP00000215882.5:p.Thr185Ile | |
| ENST00000215882.9:c.554C>T | ENSP00000215882.5:p.Thr185Ile | |
| ENST00000451283.5:c.245C>T | ENSP00000401480.1:p.Thr82Ile | |
| ENST00000461267.1:n.700C>T | ||
| ENST00000470922.5:n.696C>T | ||
| NM_001256534.1:c.575C>T | NP_001243463.1:p.Thr192Ile | |
| NM_001287387.1:c.245C>T | NP_001274316.1:p.Thr82Ile | |
| NM_005984.4:c.554C>T | NP_005975.1:p.Thr185Ile | |
| NR_046298.2:n.605C>T | ||
| NM_005984.5:c.554C>T MANE Select | NP_005975.1:p.Thr185Ile | |
| NM_001256534.2:c.575C>T | NP_001243463.1:p.Thr192Ile | |
| NM_001287387.2:c.245C>T | NP_001274316.1:p.Thr82Ile | |
| NR_046298.3:n.478C>T |