Canonical Allele Identifier: CA1804794623
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269921C= , CM000670.2:g.97269921C= GRCh38
NC_000008.10:g.98282149C= , CM000670.1:g.98282149C= GRCh37
NC_000008.9:g.98351325C= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_125390.1:n.471+149149G=