Canonical Allele Identifier: CA1250829335
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722365G= , CM000664.2:g.52722365G= GRCh38
NC_000002.11:g.52949503G= , CM000664.1:g.52949503G= GRCh37
NC_000002.10:g.52803007G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.892C=