Canonical Allele Identifier: CA2263926933
Gene:

Linked Data

dbSNP Id: rs1908569486

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211727T>C , CM000679.2:g.50211727T>C GRCh38
NC_000017.10:g.48289088T>C , CM000679.1:g.48289088T>C GRCh37
NC_000017.9:g.45644087T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2108T>C