Canonical Allele Identifier: CA11461507
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.178048676T>G , CM000665.2:g.178048676T>G GRCh38
NC_000003.11:g.177766464T>G , CM000665.1:g.177766464T>G GRCh37
NC_000003.10:g.179249158T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924739.1:n.67-248T>G
XR_001741026.1:n.115-1379T>G