Canonical Allele Identifier: CA1250829311
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722337C= , CM000664.2:g.52722337C= GRCh38
NC_000002.11:g.52949475C= , CM000664.1:g.52949475C= GRCh37
NC_000002.10:g.52802979C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.920G=