Canonical Allele Identifier:
CA647516937
Gene:
Linked Data
dbSNP Id:
rs1444345674
gnomAD v3:
2-155870599-C-A
gnomAD v4:
2-155870599-C-A
COSMIC:
COSN9863980
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.155870599C>A , CM000664.2:g.155870599C>A | GRCh38 |
| NC_000002.11:g.156727111C>A , CM000664.1:g.156727111C>A | GRCh37 |
| NC_000002.10:g.156435357C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923501.1:n.320-3412G>T | ||
| XR_001739749.1:n.331-29615G>T | ||
| XR_001739750.1:n.331-29615G>T | ||
| XR_001739751.1:n.331-29615G>T | ||
| XR_923501.2:n.331-3412G>T |