Canonical Allele Identifier: CA2166307661
Gene: OCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752083C= , CM000677.2:g.27752083C= GRCh38
NC_000015.9:g.27997229C= , CM000677.1:g.27997229C= GRCh37
NC_000015.8:g.25670824C= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32755G= XP_016877747.1:n.2457-32755G=
XM_017022264.1:c.2292-32755G= XP_016877753.1:n.2292-32755G=