Canonical Allele Identifier: CA267898286

Gene: OCA2

Linked Data

• dbSNP Id: rs56141333
• gnomAD v2: 15-28338557-CA-C
• gnomAD v3: 15-28093411-CA-C
• gnomAD v4: 15-28093411-CA-C
• MyVariant Identifiers: chr15:g.28338560del (hg19) ; chr15:g.28338558del (hg19) ; chr15:g.28093414del (hg38) ; chr15:g.28093412del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28093424del , CM000677.2:g.28093424del	GRCh38
NC_000015.9:g.28338570del , CM000677.1:g.28338570del	GRCh37
NC_000015.8:g.26012165del	NCBI36
NG_009846.1:g.10901del

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.-22+5812del MANE Select	ENSP00000346659.3:n.-22+5812del
ENST00000353809.9:c.-22+5812del	ENSP00000261276.8:n.-22+5812del
ENST00000354638.7:c.-22+5812del	ENSP00000346659.3:n.-22+5812del
ENST00000431101.1:c.-22+5699del	ENSP00000415431.1:n.-22+5699del
ENST00000445578.5:c.-22+5812del	ENSP00000414425.1:n.-22+5812del
NM_000275.2:c.-22+5812del	NP_000266.2:n.-22+5812del
NM_001300984.1:c.-22+5812del	NP_001287913.1:n.-22+5812del
XM_011521640.1:c.-22+5812del	XP_011519942.1:n.-22+5812del
XM_011521640.2:c.-22+5812del	XP_011519942.1:n.-22+5812del
NM_000275.3:c.-22+5812del MANE Select	NP_000266.2:n.-22+5812del
NM_001300984.2:c.-22+5812del	NP_001287913.1:n.-22+5812del