Canonical Allele Identifier: CA2255111865
Gene:

Linked Data

dbSNP Id: rs994841625

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237182T>C , CM000679.2:g.30237182T>C GRCh38
NC_000017.10:g.28564200T>C , CM000679.1:g.28564200T>C GRCh37
NC_000017.9:g.25588326T>C NCBI36
NG_011747.2:g.3755A>G

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+112T>C
XR_001752824.1:n.280+112T>C