Canonical Allele Identifier: CA2008080811
Gene:

Linked Data

dbSNP Id: rs1861798022

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.128455628G>C , CM000673.2:g.128455628G>C GRCh38
NC_000011.9:g.128325523G>C , CM000673.1:g.128325523G>C GRCh37
NC_000011.8:g.127830733G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948164.1:n.4348G>C
XR_948165.1:n.3467+881G>C