Canonical Allele Identifier: CA1250829352
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722391C= , CM000664.2:g.52722391C= GRCh38
NC_000002.11:g.52949529C= , CM000664.1:g.52949529C= GRCh37
NC_000002.10:g.52803033C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.866G=