Canonical Allele Identifier: CA391360031

Gene: OCA2

Linked Data

• MyVariant Identifiers: chr15:g.28096559C>A (hg19) ; chr15:g.27851413C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27851413C>A , CM000677.2:g.27851413C>A	GRCh38
NC_000015.9:g.28096559C>A , CM000677.1:g.28096559C>A	GRCh37
NC_000015.8:g.25770154C>A	NCBI36
NG_009846.1:g.252900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.2307G>T MANE Select	ENSP00000346659.3:p.Met769Ile
ENST00000353809.9:c.2235G>T	ENSP00000261276.8:p.Met745Ile
ENST00000354638.7:c.2307G>T	ENSP00000346659.3:p.Met769Ile
NM_000275.2:c.2307G>T	NP_000266.2:p.Met769Ile
NM_001300984.1:c.2235G>T	NP_001287913.1:p.Met745Ile
XM_011521639.1:c.2373G>T	XP_011519941.1:p.Met791Ile
XM_011521640.1:c.2349G>T	XP_011519942.1:p.Met783Ile
XM_011521641.1:c.2331G>T	XP_011519943.1:p.Met777Ile
XM_011521642.1:c.2301G>T	XP_011519944.1:p.Met767Ile
XM_011521643.1:c.2259G>T	XP_011519945.1:p.Met753Ile
XM_011521644.1:c.2235G>T	XP_011519946.1:p.Met745Ile
XM_011521645.1:c.2166G>T	XP_011519947.1:p.Met722Ile
XM_011521640.2:c.2349G>T	XP_011519942.1:p.Met783Ile
XM_017022255.1:c.2373G>T	XP_016877744.1:p.Met791Ile
XM_017022256.1:c.2331G>T	XP_016877745.1:p.Met777Ile
XM_017022257.1:c.2301G>T	XP_016877746.1:p.Met767Ile
XM_017022258.1:c.2331G>T	XP_016877747.1:p.Met777Ile
XM_017022259.1:c.2259G>T	XP_016877748.1:p.Met753Ile
XM_017022260.1:c.2235G>T	XP_016877749.1:p.Met745Ile
XM_017022261.1:c.2178G>T	XP_016877750.1:p.Met726Ile
XM_017022262.1:c.2268+19741G>T	XP_016877751.1:n.2268+19741G>T
XM_017022263.1:c.2166G>T	XP_016877752.1:p.Met722Ile
XM_017022264.1:c.2166G>T	XP_016877753.1:p.Met722Ile
NM_000275.3:c.2307G>T MANE Select	NP_000266.2:p.Met769Ile
NM_001300984.2:c.2235G>T	NP_001287913.1:p.Met745Ile