Canonical Allele Identifier: CA2502528420
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.195007162G>A , CM000664.2:g.195007162G>A GRCh38
NC_000002.11:g.195871886G>A , CM000664.1:g.195871886G>A GRCh37
NC_000002.10:g.195580131G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739836.1:n.553+52273C>T