Canonical Allele Identifier: CA909861235
Gene:

Linked Data

dbSNP Id: rs1222943537

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.70577141A>C , CM000665.2:g.70577141A>C GRCh38
NC_000003.11:g.70626292A>C , CM000665.1:g.70626292A>C GRCh37
NC_000003.10:g.70708982A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940947.1:n.407-1188T>G
XR_001740559.1:n.367-1188T>G