Canonical Allele Identifier: CA711703725
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1441615429
gnomAD v3: 15-27752087-G-A
gnomAD v4: 15-27752087-G-A
MyVariant Identifiers: chr15:g.27997233G>A (hg19) chr15:g.27752087G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752087G>A , CM000677.2:g.27752087G>A GRCh38
NC_000015.9:g.27997233G>A , CM000677.1:g.27997233G>A GRCh37
NC_000015.8:g.25670828G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017022258.1:c.2457-32759C>T XP_016877747.1:n.2457-32759C>T
XM_017022264.1:c.2292-32759C>T XP_016877753.1:n.2292-32759C>T
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