Canonical Allele Identifier: CA1250829326
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722355G= , CM000664.2:g.52722355G= GRCh38
NC_000002.11:g.52949493G= , CM000664.1:g.52949493G= GRCh37
NC_000002.10:g.52802997G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.902C=