Canonical Allele Identifier: CA2341104178
Gene:

Linked Data

dbSNP Id: rs2090049901

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837461G>T , CM000681.2:g.50837461G>T GRCh38
NC_000019.9:g.51340717G>T , CM000681.1:g.51340717G>T GRCh37
NC_000019.8:g.56032529G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6168G>T
NR_131205.1:n.230+6168G>T
XR_936030.1:n.298+6168G>T
XR_936031.1:n.298+6168G>T
XR_936032.1:n.298+6168G>T
XR_936033.1:n.294+6168G>T
XR_936035.1:n.281+6168G>T