Canonical Allele Identifier: CA1361514976
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.45075681A>T , CM000665.2:g.45075681A>T GRCh38
NC_000003.11:g.45117173A>T , CM000665.1:g.45117173A>T GRCh37
NC_000003.10:g.45092177A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940792.1:n.325+5572A>T
XR_940793.1:n.239-5972A>T
XR_940794.1:n.325+5572A>T