Canonical Allele Identifier: CA2343599302
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.55754333C= , CM000681.2:g.55754333C= GRCh38
NC_000019.9:g.56265699C= , CM000681.1:g.56265699C= GRCh37
NC_000019.8:g.60957511C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_936081.1:n.202C=
XR_936081.2:n.261C=