Canonical Allele Identifier: CA13664778
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28040056G>A , CM000674.2:g.28040056G>A GRCh38
NC_000012.11:g.28192989G>A , CM000674.1:g.28192989G>A GRCh37
NC_000012.10:g.28084256G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931460.1:n.154-1098C>T