Canonical Allele Identifier: CA1250829399
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722448G= , CM000664.2:g.52722448G= GRCh38
NC_000002.11:g.52949586G= , CM000664.1:g.52949586G= GRCh37
NC_000002.10:g.52803090G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.809C=