Canonical Allele Identifier: CA268293527
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs180996141
gnomAD v2: 15-27997341-T-C
gnomAD v3: 15-27752195-T-C
gnomAD v4: 15-27752195-T-C
MyVariant Identifiers: chr15:g.27997341T>C (hg19) chr15:g.27752195T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752195T>C , CM000677.2:g.27752195T>C GRCh38
NC_000015.9:g.27997341T>C , CM000677.1:g.27997341T>C GRCh37
NC_000015.8:g.25670936T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017022258.1:c.2457-32867A>G XP_016877747.1:n.2457-32867A>G
XM_017022264.1:c.2292-32867A>G XP_016877753.1:n.2292-32867A>G
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