Canonical Allele Identifier: CA2753721063
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007177T>A , CM000664.2:g.195007177T>A GRCh38
NC_000002.11:g.195871901T>A , CM000664.1:g.195871901T>A GRCh37
NC_000002.10:g.195580146T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001739836.1:n.553+52258A>T