Canonical Allele Identifier: CA655861733
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2030084367

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752111G>A , CM000677.2:g.27752111G>A GRCh38
NC_000015.9:g.27997257G>A , CM000677.1:g.27997257G>A GRCh37
NC_000015.8:g.25670852G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017022258.1:c.2457-32783C>T XP_016877747.1:n.2457-32783C>T
XM_017022264.1:c.2292-32783C>T XP_016877753.1:n.2292-32783C>T