Canonical Allele Identifier: CA1038177623
Gene:

Linked Data

dbSNP Id: rs1683152950

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870727A>C , CM000664.2:g.155870727A>C GRCh38
NC_000002.11:g.156727239A>C , CM000664.1:g.156727239A>C GRCh37
NC_000002.10:g.156435485A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3540T>G
XR_001739749.1:n.331-29743T>G
XR_001739750.1:n.331-29743T>G
XR_001739751.1:n.331-29743T>G
XR_923501.2:n.331-3540T>G