Canonical Allele Identifier: CA625447426
Gene:

Linked Data

dbSNP Id: rs1292241733

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237241G>C , CM000679.2:g.30237241G>C GRCh38
NC_000017.10:g.28564259G>C , CM000679.1:g.28564259G>C GRCh37
NC_000017.9:g.25588385G>C NCBI36
NG_011747.2:g.3696C>G

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+171G>C
XR_001752824.1:n.280+171G>C