Canonical Allele Identifier: CA16156077
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.120866468C>T , CM000665.2:g.120866468C>T GRCh38
NC_000003.11:g.120585315C>T , CM000665.1:g.120585315C>T GRCh37
NC_000003.10:g.122068005C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924398.1:n.658+1801G>A
XR_924399.1:n.415+1801G>A
XR_924398.3:n.658+1801G>A
XR_924399.3:n.415+1801G>A