Canonical Allele Identifier: CA2255111878
Gene:

Linked Data

dbSNP Id: rs1597650277

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237196T>C , CM000679.2:g.30237196T>C GRCh38
NC_000017.10:g.28564214T>C , CM000679.1:g.28564214T>C GRCh37
NC_000017.9:g.25588340T>C NCBI36
NG_011747.2:g.3741A>G

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+126T>C
XR_001752824.1:n.280+126T>C