Canonical Allele Identifier: CA1889304373
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.8659170A= , CM000672.2:g.8659170A= GRCh38
NC_000010.10:g.8701133A= , CM000672.1:g.8701133A= GRCh37
NC_000010.9:g.8741139A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930641.1:n.178T=
XR_001747277.1:n.147T=