Canonical Allele Identifier: CA11535399
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.106193283T>C , CM000665.2:g.106193283T>C GRCh38
NC_000003.11:g.105912130T>C , CM000665.1:g.105912130T>C GRCh37
NC_000003.10:g.107394820T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_924311.1:n.176-517T>C
XR_924312.1:n.176-9231T>C
XR_924311.2:n.176-517T>C