Canonical Allele Identifier: CA2581059238
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.80851695G>T , CM000673.2:g.80851695G>T GRCh38
NC_000011.9:g.80562738G>T , CM000673.1:g.80562738G>T GRCh37
NC_000011.8:g.80240386G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_247272.2:n.124+60596C>A