Canonical Allele Identifier: CA1889304377
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8659172G= , CM000672.2:g.8659172G= GRCh38
NC_000010.10:g.8701135G= , CM000672.1:g.8701135G= GRCh37
NC_000010.9:g.8741141G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.176C=
XR_001747277.1:n.145C=