Canonical Allele Identifier: CA1373743890
Gene:

Linked Data

dbSNP Id: rs1265108915

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577111C>G , CM000665.2:g.70577111C>G GRCh38
NC_000003.11:g.70626262C>G , CM000665.1:g.70626262C>G GRCh37
NC_000003.10:g.70708952C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940947.1:n.407-1158G>C
XR_001740559.1:n.367-1158G>C