Canonical Allele Identifier: CA178101914
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60049262G>T , CM000670.2:g.60049262G>T GRCh38
NC_000008.10:g.60961821G>T , CM000670.1:g.60961821G>T GRCh37
NC_000008.9:g.61124375G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928932.1:n.156-264G>T
XR_001745714.2:n.184-264G>T
XR_001745716.2:n.184-264G>T
XR_001745717.2:n.156-264G>T
XR_002956710.1:n.184-264G>T
XR_002956711.1:n.156-264G>T