Canonical Allele Identifier: CA2255112064
Gene:

Linked Data

dbSNP Id: rs1907329058

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237374G>C , CM000679.2:g.30237374G>C GRCh38
NC_000017.10:g.28564392G>C , CM000679.1:g.28564392G>C GRCh37
NC_000017.9:g.25588518G>C NCBI36
NG_011747.2:g.3563C>G

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.166-268G>C
XR_001752824.1:n.281-268G>C