Canonical Allele Identifier: CA2723115885
Gene:

Linked Data

dbSNP Id: rs1845998461

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.2444567G>A , CM000673.2:g.2444567G>A GRCh38
NC_000011.9:g.2465797G>A , CM000673.1:g.2465797G>A GRCh37
NC_000011.8:g.2422373G>A NCBI36
NG_008935.1:g.4577G>A , LRG_287:g.4577G>A

Transcript Alleles

HGVS Amino-acid Change
XR_930984.1:n.4C>T