Canonical Allele Identifier: CA616999732
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1404224712
gnomAD v2: 15-27997278-CA-C
gnomAD v3: 15-27752132-CA-C
gnomAD v4: 15-27752132-CA-C
MyVariant Identifiers: chr15:g.27997279del (hg19) chr15:g.27752133del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752134del , CM000677.2:g.27752134del GRCh38
NC_000015.9:g.27997280del , CM000677.1:g.27997280del GRCh37
NC_000015.8:g.25670875del NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32805del XP_016877747.1:n.2457-32805del
XM_017022264.1:c.2292-32805del XP_016877753.1:n.2292-32805del
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