Canonical Allele Identifier: CA2529265630
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122883853A>C , CM000664.2:g.122883853A>C GRCh38
NC_000002.11:g.123641429A>C , CM000664.1:g.123641429A>C GRCh37
NC_000002.10:g.123357899A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923292.1:n.1125-1089A>C
XR_001739692.1:n.1451-1089A>C
XR_923292.2:n.1358-1089A>C