Canonical Allele Identifier: CA2255111988
Gene:

Linked Data

dbSNP Id: rs1336477427

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237301A>C , CM000679.2:g.30237301A>C GRCh38
NC_000017.10:g.28564319A>C , CM000679.1:g.28564319A>C GRCh37
NC_000017.9:g.25588445A>C NCBI36
NG_011747.2:g.3636T>G

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+231A>C
XR_001752824.1:n.280+231A>C