Canonical Allele Identifier: CA268293495
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs192533082
gnomAD v2: 15-27997126-T-C
gnomAD v3: 15-27751980-T-C
gnomAD v4: 15-27751980-T-C
MyVariant Identifiers: chr15:g.27997126T>C (hg19) chr15:g.27751980T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27751980T>C , CM000677.2:g.27751980T>C GRCh38
NC_000015.9:g.27997126T>C , CM000677.1:g.27997126T>C GRCh37
NC_000015.8:g.25670721T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32652A>G XP_016877747.1:n.2457-32652A>G
XM_017022264.1:c.2292-32652A>G XP_016877753.1:n.2292-32652A>G
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