Canonical Allele Identifier: CA268293508
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs80237933
gnomAD v2: 15-27997238-C-T
gnomAD v3: 15-27752092-C-T
gnomAD v4: 15-27752092-C-T
MyVariant Identifiers: chr15:g.27997238C>T (hg19) chr15:g.27752092C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752092C>T , CM000677.2:g.27752092C>T GRCh38
NC_000015.9:g.27997238C>T , CM000677.1:g.27997238C>T GRCh37
NC_000015.8:g.25670833C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_017022258.1:c.2457-32764G>A XP_016877747.1:n.2457-32764G>A
XM_017022264.1:c.2292-32764G>A XP_016877753.1:n.2292-32764G>A
Search 100 bp 5'
Search 100 bp 3'