Canonical Allele Identifier: CA2166307647
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1595353972

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752049G>C , CM000677.2:g.27752049G>C GRCh38
NC_000015.9:g.27997195G>C , CM000677.1:g.27997195G>C GRCh37
NC_000015.8:g.25670790G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32721C>G XP_016877747.1:n.2457-32721C>G
XM_017022264.1:c.2292-32721C>G XP_016877753.1:n.2292-32721C>G