Canonical Allele Identifier: CA982865653
Gene:

Linked Data

dbSNP Id: rs1168870912

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237207C>A , CM000679.2:g.30237207C>A GRCh38
NC_000017.10:g.28564225C>A , CM000679.1:g.28564225C>A GRCh37
NC_000017.9:g.25588351C>A NCBI36
NG_011747.2:g.3730G>T

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+137C>A
XR_001752824.1:n.280+137C>A