Canonical Allele Identifier: CA2493232111
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20485751G= , CM000664.2:g.20485751G= GRCh38
NC_000002.11:g.20685512G= , CM000664.1:g.20685512G= GRCh37
NC_000002.10:g.20548993G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_157978.1:n.530+2987C=