Canonical Allele Identifier: CA2535698364
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722338C>A , CM000664.2:g.52722338C>A GRCh38
NC_000002.11:g.52949476C>A , CM000664.1:g.52949476C>A GRCh37
NC_000002.10:g.52802980C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.919G>T