Canonical Allele Identifier: CA267893653

Gene: OCA2

Linked Data

• dbSNP Id: rs562134779
• gnomAD v3: 15-27990595-G-C
• gnomAD v4: 15-27990595-G-C
• MyVariant Identifiers: chr15:g.28235741G>C (hg19) ; chr15:g.27990595G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27990595G>C , CM000677.2:g.27990595G>C	GRCh38
NC_000015.9:g.28235741G>C , CM000677.1:g.28235741G>C	GRCh37
NC_000015.8:g.25909336G>C	NCBI36
NG_009846.1:g.113718C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.1097C>G MANE Select	ENSP00000346659.3:p.Ala366Gly
ENST00000353809.9:c.1045-929C>G	ENSP00000261276.8:n.1045-929C>G
ENST00000354638.7:c.1097C>G	ENSP00000346659.3:p.Ala366Gly
NM_000275.2:c.1097C>G	NP_000266.2:p.Ala366Gly
NM_001300984.1:c.1045-929C>G	NP_001287913.1:n.1045-929C>G
XM_011521639.1:c.1121C>G	XP_011519941.1:p.Ala374Gly
XM_011521640.1:c.1097C>G	XP_011519942.1:p.Ala366Gly
XM_011521641.1:c.1121C>G	XP_011519943.1:p.Ala374Gly
XM_011521642.1:c.1069-929C>G	XP_011519944.1:n.1069-929C>G
XM_011521643.1:c.1069-929C>G	XP_011519945.1:n.1069-929C>G
XM_011521644.1:c.1069-3952C>G	XP_011519946.1:n.1069-3952C>G
XM_011521645.1:c.1121C>G	XP_011519947.1:p.Ala374Gly
XM_011521646.1:c.1121C>G	XP_011519948.1:p.Ala374Gly
XM_011521647.1:c.1121C>G	XP_011519949.1:p.Ala374Gly
XR_931843.1:n.2482C>G
XM_011521640.2:c.1097C>G	XP_011519942.1:p.Ala366Gly
XM_017022255.1:c.1121C>G	XP_016877744.1:p.Ala374Gly
XM_017022256.1:c.1121C>G	XP_016877745.1:p.Ala374Gly
XM_017022257.1:c.1069-929C>G	XP_016877746.1:n.1069-929C>G
XM_017022258.1:c.1121C>G	XP_016877747.1:p.Ala374Gly
XM_017022259.1:c.1069-929C>G	XP_016877748.1:n.1069-929C>G
XM_017022260.1:c.1069-3952C>G	XP_016877749.1:n.1069-3952C>G
XM_017022261.1:c.926C>G	XP_016877750.1:p.Ala309Gly
XM_017022262.1:c.1121C>G	XP_016877751.1:p.Ala374Gly
XM_017022263.1:c.1121C>G	XP_016877752.1:p.Ala374Gly
XM_017022264.1:c.1121C>G	XP_016877753.1:p.Ala374Gly
XM_017022265.1:c.1121C>G	XP_016877754.1:p.Ala374Gly
XR_001751294.1:n.1210C>G
NM_000275.3:c.1097C>G MANE Select	NP_000266.2:p.Ala366Gly
NM_001300984.2:c.1045-929C>G	NP_001287913.1:n.1045-929C>G