Canonical Allele Identifier: CA2341104239
Gene:

Linked Data

dbSNP Id: rs955062118

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837577C>G , CM000681.2:g.50837577C>G GRCh38
NC_000019.9:g.51340833C>G , CM000681.1:g.51340833C>G GRCh37
NC_000019.8:g.56032645C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6284C>G
NR_131205.1:n.230+6284C>G
XR_936030.1:n.298+6284C>G
XR_936031.1:n.298+6284C>G
XR_936032.1:n.298+6284C>G
XR_936033.1:n.294+6284C>G
XR_936035.1:n.281+6284C>G