Canonical Allele Identifier: CA616999727
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1190938869
gnomAD v2: 15-27997190-A-G
gnomAD v3: 15-27752044-A-G
gnomAD v4: 15-27752044-A-G
MyVariant Identifiers: chr15:g.27997190A>G (hg19) chr15:g.27752044A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752044A>G , CM000677.2:g.27752044A>G GRCh38
NC_000015.9:g.27997190A>G , CM000677.1:g.27997190A>G GRCh37
NC_000015.8:g.25670785A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32716T>C XP_016877747.1:n.2457-32716T>C
XM_017022264.1:c.2292-32716T>C XP_016877753.1:n.2292-32716T>C
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