Canonical Allele Identifier: CA391361042

Gene: OCA2

Linked Data

• gnomAD v4: 15-27926162-G-C
• MyVariant Identifiers: chr15:g.28171308G>C (hg19) ; chr15:g.27926162G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926162G>C , CM000677.2:g.27926162G>C	GRCh38
NC_000015.9:g.28171308G>C , CM000677.1:g.28171308G>C	GRCh37
NC_000015.8:g.25844903G>C	NCBI36
NG_009846.1:g.178151C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.2044C>G MANE Select	ENSP00000346659.3:p.Leu682Val
ENST00000353809.9:c.1972C>G	ENSP00000261276.8:p.Leu658Val
ENST00000354638.7:c.2044C>G	ENSP00000346659.3:p.Leu682Val
NM_000275.2:c.2044C>G	NP_000266.2:p.Leu682Val
NM_001300984.1:c.1972C>G	NP_001287913.1:p.Leu658Val
XM_011521639.1:c.2068C>G	XP_011519941.1:p.Leu690Val
XM_011521640.1:c.2044C>G	XP_011519942.1:p.Leu682Val
XM_011521641.1:c.2068C>G	XP_011519943.1:p.Leu690Val
XM_011521642.1:c.1996C>G	XP_011519944.1:p.Leu666Val
XM_011521643.1:c.1996C>G	XP_011519945.1:p.Leu666Val
XM_011521644.1:c.1930C>G	XP_011519946.1:p.Leu644Val
XM_011521645.1:c.2068C>G	XP_011519947.1:p.Leu690Val
XM_011521640.2:c.2044C>G	XP_011519942.1:p.Leu682Val
XM_017022255.1:c.2068C>G	XP_016877744.1:p.Leu690Val
XM_017022256.1:c.2068C>G	XP_016877745.1:p.Leu690Val
XM_017022257.1:c.1996C>G	XP_016877746.1:p.Leu666Val
XM_017022258.1:c.2068C>G	XP_016877747.1:p.Leu690Val
XM_017022259.1:c.1996C>G	XP_016877748.1:p.Leu666Val
XM_017022260.1:c.1930C>G	XP_016877749.1:p.Leu644Val
XM_017022261.1:c.1873C>G	XP_016877750.1:p.Leu625Val
XM_017022262.1:c.2068C>G	XP_016877751.1:p.Leu690Val
XM_017022263.1:c.2068C>G	XP_016877752.1:p.Leu690Val
XM_017022264.1:c.2068C>G	XP_016877753.1:p.Leu690Val
NM_000275.3:c.2044C>G MANE Select	NP_000266.2:p.Leu682Val
NM_001300984.2:c.1972C>G	NP_001287913.1:p.Leu658Val