Canonical Allele Identifier: CA2581059237
Gene:

Genomic Alleles

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

Transcript Alleles

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