Canonical Allele Identifier: CA1595159119
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580773T= , CM000667.2:g.159580773T= GRCh38
NC_000005.9:g.159007781T= , CM000667.1:g.159007781T= GRCh37
NC_000005.8:g.158940359T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+338T=
XR_941140.1:n.2075+338T=
XR_941141.1:n.570+338T=
XR_941139.2:n.2229+338T=