Canonical Allele Identifier: CA287548459
Gene:

Linked Data

dbSNP Id: rs950292978

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137282A>C , CM000679.2:g.8137282A>C GRCh38
NC_000017.10:g.8040600A>C , CM000679.1:g.8040600A>C GRCh37
NC_000017.9:g.7981325A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1567A>C
XR_934203.1:n.70-2195A>C
XR_934202.2:n.414-1567A>C