Canonical Allele Identifier: CA1161925206
Gene:

Linked Data

dbSNP Id: rs1171527845

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.34523554C>G , CM000663.2:g.34523554C>G GRCh38
NC_000001.10:g.34989155C>G , CM000663.1:g.34989155C>G GRCh37
NC_000001.9:g.34761742C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_947171.1:n.1073+24025G>C
XR_001737964.1:n.991+24025G>C