Canonical Allele Identifier: CA268293500
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs138377043

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752022G>C , CM000677.2:g.27752022G>C GRCh38
NC_000015.9:g.27997168G>C , CM000677.1:g.27997168G>C GRCh37
NC_000015.8:g.25670763G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32694C>G XP_016877747.1:n.2457-32694C>G
XM_017022264.1:c.2292-32694C>G XP_016877753.1:n.2292-32694C>G