Canonical Allele Identifier: CA2166307632
Gene: OCA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752020T= , CM000677.2:g.27752020T= GRCh38
NC_000015.9:g.27997166T= , CM000677.1:g.27997166T= GRCh37
NC_000015.8:g.25670761T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32692A= XP_016877747.1:n.2457-32692A=
XM_017022264.1:c.2292-32692A= XP_016877753.1:n.2292-32692A=