Canonical Allele Identifier: CA268293499
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs146263170

Genomic Alleles

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

Transcript Alleles

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