Canonical Allele Identifier: CA2814739491
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837741A>C , CM000681.2:g.50837741A>C GRCh38
NC_000019.9:g.51340997A>C , CM000681.1:g.51340997A>C GRCh37
NC_000019.8:g.56032809A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_131203.1:n.213+6448A>C
NR_131205.1:n.230+6448A>C
XR_936030.1:n.298+6448A>C
XR_936031.1:n.298+6448A>C
XR_936032.1:n.298+6448A>C
XR_936033.1:n.294+6448A>C
XR_936035.1:n.281+6448A>C