Canonical Allele Identifier: CA2246165656
Gene:

Linked Data

dbSNP Id: rs1598240828

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8137311A>C , CM000679.2:g.8137311A>C GRCh38
NC_000017.10:g.8040629A>C , CM000679.1:g.8040629A>C GRCh37
NC_000017.9:g.7981354A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934202.1:n.183-1538A>C
XR_934203.1:n.70-2166A>C
XR_934202.2:n.414-1538A>C