Canonical Allele Identifier: CA391361401

Gene: OCA2

Linked Data

• gnomAD v4: 15-27926242-A-G
• MyVariant Identifiers: chr15:g.28171388A>G (hg19) ; chr15:g.27926242A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.27926242A>G , CM000677.2:g.27926242A>G	GRCh38
NC_000015.9:g.28171388A>G , CM000677.1:g.28171388A>G	GRCh37
NC_000015.8:g.25844983A>G	NCBI36
NG_009846.1:g.178071T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.1964T>C MANE Select	ENSP00000346659.3:p.Ile655Thr
ENST00000353809.9:c.1892T>C	ENSP00000261276.8:p.Ile631Thr
ENST00000354638.7:c.1964T>C	ENSP00000346659.3:p.Ile655Thr
NM_000275.2:c.1964T>C	NP_000266.2:p.Ile655Thr
NM_001300984.1:c.1892T>C	NP_001287913.1:p.Ile631Thr
XM_011521639.1:c.1988T>C	XP_011519941.1:p.Ile663Thr
XM_011521640.1:c.1964T>C	XP_011519942.1:p.Ile655Thr
XM_011521641.1:c.1988T>C	XP_011519943.1:p.Ile663Thr
XM_011521642.1:c.1916T>C	XP_011519944.1:p.Ile639Thr
XM_011521643.1:c.1916T>C	XP_011519945.1:p.Ile639Thr
XM_011521644.1:c.1850T>C	XP_011519946.1:p.Ile617Thr
XM_011521645.1:c.1988T>C	XP_011519947.1:p.Ile663Thr
XM_011521640.2:c.1964T>C	XP_011519942.1:p.Ile655Thr
XM_017022255.1:c.1988T>C	XP_016877744.1:p.Ile663Thr
XM_017022256.1:c.1988T>C	XP_016877745.1:p.Ile663Thr
XM_017022257.1:c.1916T>C	XP_016877746.1:p.Ile639Thr
XM_017022258.1:c.1988T>C	XP_016877747.1:p.Ile663Thr
XM_017022259.1:c.1916T>C	XP_016877748.1:p.Ile639Thr
XM_017022260.1:c.1850T>C	XP_016877749.1:p.Ile617Thr
XM_017022261.1:c.1793T>C	XP_016877750.1:p.Ile598Thr
XM_017022262.1:c.1988T>C	XP_016877751.1:p.Ile663Thr
XM_017022263.1:c.1988T>C	XP_016877752.1:p.Ile663Thr
XM_017022264.1:c.1988T>C	XP_016877753.1:p.Ile663Thr
NM_000275.3:c.1964T>C MANE Select	NP_000266.2:p.Ile655Thr
NM_001300984.2:c.1892T>C	NP_001287913.1:p.Ile631Thr