Canonical Allele Identifier: CA2581395954
Gene:

Genomic Alleles

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

Transcript Alleles

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