Canonical Allele Identifier: CA2341104194
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.50837488A= , CM000681.2:g.50837488A= GRCh38
NC_000019.9:g.51340744A= , CM000681.1:g.51340744A= GRCh37
NC_000019.8:g.56032556A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_131203.1:n.213+6195A=
NR_131205.1:n.230+6195A=
XR_936030.1:n.298+6195A=
XR_936031.1:n.298+6195A=
XR_936032.1:n.298+6195A=
XR_936033.1:n.294+6195A=
XR_936035.1:n.281+6195A=