Canonical Allele Identifier: CA2504219275
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.52722395G>T , CM000664.2:g.52722395G>T GRCh38
NC_000002.11:g.52949533G>T , CM000664.1:g.52949533G>T GRCh37
NC_000002.10:g.52803037G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_002959384.1:n.862C>A