Canonical Allele Identifier: CA2166307642
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2030081502

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752042G>A , CM000677.2:g.27752042G>A GRCh38
NC_000015.9:g.27997188G>A , CM000677.1:g.27997188G>A GRCh37
NC_000015.8:g.25670783G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32714C>T XP_016877747.1:n.2457-32714C>T
XM_017022264.1:c.2292-32714C>T XP_016877753.1:n.2292-32714C>T