Canonical Allele Identifier: CA1769514579
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735011C= , CM000670.2:g.20735011C= GRCh38
NC_000008.10:g.20592522C= , CM000670.1:g.20592522C= GRCh37
NC_000008.9:g.20636802C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55435C=