Canonical Allele Identifier: CA309668933
Gene:

Linked Data

dbSNP Id: rs565991137

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837481A>G , CM000681.2:g.50837481A>G GRCh38
NC_000019.9:g.51340737A>G , CM000681.1:g.51340737A>G GRCh37
NC_000019.8:g.56032549A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6188A>G
NR_131205.1:n.230+6188A>G
XR_936030.1:n.298+6188A>G
XR_936031.1:n.298+6188A>G
XR_936032.1:n.298+6188A>G
XR_936033.1:n.294+6188A>G
XR_936035.1:n.281+6188A>G