Canonical Allele Identifier: CA657517629
Gene:

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837719A>T , CM000681.2:g.50837719A>T GRCh38
NC_000019.9:g.51340975A>T , CM000681.1:g.51340975A>T GRCh37
NC_000019.8:g.56032787A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6426A>T
NR_131205.1:n.230+6426A>T
XR_936030.1:n.298+6426A>T
XR_936031.1:n.298+6426A>T
XR_936032.1:n.298+6426A>T
XR_936033.1:n.294+6426A>T
XR_936035.1:n.281+6426A>T