Canonical Allele Identifier: CA309668904
Gene:

Linked Data

dbSNP Id: rs1052337357

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837416G>T , CM000681.2:g.50837416G>T GRCh38
NC_000019.9:g.51340672G>T , CM000681.1:g.51340672G>T GRCh37
NC_000019.8:g.56032484G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6123G>T
NR_131205.1:n.230+6123G>T
XR_936030.1:n.298+6123G>T
XR_936031.1:n.298+6123G>T
XR_936032.1:n.298+6123G>T
XR_936033.1:n.294+6123G>T
XR_936035.1:n.281+6123G>T