Canonical Allele Identifier: CA2166307605
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2030078547

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27751940C>T , CM000677.2:g.27751940C>T GRCh38
NC_000015.9:g.27997086C>T , CM000677.1:g.27997086C>T GRCh37
NC_000015.8:g.25670681C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32612G>A XP_016877747.1:n.2457-32612G>A
XM_017022264.1:c.2292-32612G>A XP_016877753.1:n.2292-32612G>A