Canonical Allele Identifier: CA2343599288
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55754298A= , CM000681.2:g.55754298A= GRCh38
NC_000019.9:g.56265664A= , CM000681.1:g.56265664A= GRCh37
NC_000019.8:g.60957476A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936081.1:n.167A=
XR_936081.2:n.226A=