Canonical Allele Identifier: CA1261549156
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.74711991C= , CM000664.2:g.74711991C= GRCh38
NC_000002.11:g.74939118C= , CM000664.1:g.74939118C= GRCh37
NC_000002.10:g.74792626C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427047.4:n.304C=