Canonical Allele Identifier: CA2607232867
Gene:

Linked Data

dbSNP Id: rs2102651335

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220491619G>A , CM000663.2:g.220491619G>A GRCh38
NC_000001.10:g.220664961G>A , CM000663.1:g.220664961G>A GRCh37
NC_000001.9:g.218731584G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922615.1:n.256-615G>A
XR_001737822.1:n.557-615G>A