Canonical Allele Identifier: CA2166307601
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs2030078357

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27751930A>G , CM000677.2:g.27751930A>G GRCh38
NC_000015.9:g.27997076A>G , CM000677.1:g.27997076A>G GRCh37
NC_000015.8:g.25670671A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32602T>C XP_016877747.1:n.2457-32602T>C
XM_017022264.1:c.2292-32602T>C XP_016877753.1:n.2292-32602T>C