Canonical Allele Identifier: CA1373743917
Gene:

Linked Data

dbSNP Id: rs1701574155

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577121A>G , CM000665.2:g.70577121A>G GRCh38
NC_000003.11:g.70626272A>G , CM000665.1:g.70626272A>G GRCh37
NC_000003.10:g.70708962A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1168T>C
XR_001740559.1:n.367-1168T>C