Canonical Allele Identifier: CA2713142530
Gene:

Linked Data

dbSNP Id: rs1182878129

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812277A>C , CM000668.2:g.155812277A>C GRCh38
NC_000006.11:g.156133411A>C , CM000668.1:g.156133411A>C GRCh37
NC_000006.10:g.156175103A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18858A>C
XR_943146.1:n.645-238T>G
XR_001744423.1:n.699-238T>G
XR_001744424.1:n.79+18858A>C