Canonical Allele Identifier: CA616999733
Gene: OCA2 HGNC NCBI

Linked Data

dbSNP Id: rs1369449479
gnomAD v2: 15-27997302-C-T
gnomAD v3: 15-27752156-C-T
gnomAD v4: 15-27752156-C-T
MyVariant Identifiers: chr15:g.27997302C>T (hg19) chr15:g.27752156C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.27752156C>T , CM000677.2:g.27752156C>T GRCh38
NC_000015.9:g.27997302C>T , CM000677.1:g.27997302C>T GRCh37
NC_000015.8:g.25670897C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_017022258.1:c.2457-32828G>A XP_016877747.1:n.2457-32828G>A
XM_017022264.1:c.2292-32828G>A XP_016877753.1:n.2292-32828G>A
Search 100 bp 5'
Search 100 bp 3'