Canonical Allele Identifier: CA450758862

Gene: EYS

Linked Data

• ClinVar Variation Id: 2990148
• ClinVar RCV Id: RCV003844843
• gnomAD v4: 6-64230761-C-T
• MyVariant Identifiers: chr6:g.64940654C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230761C>T , CM000668.2:g.64230761C>T	GRCh38
NC_000006.11:g.64940654C>T , CM000668.1:g.64940654C>T	GRCh37
NC_000006.10:g.64998613C>T	NCBI36
NG_023443.1:g.1481465G>A
NG_023443.2:g.1481465G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6255G>A MANE Select	ENSP00000424243.1:p.Gly2085=
ENST00000370616.6:c.6255G>A	ENSP00000359650.2:p.Gly2085=
ENST00000370618.7:c.6255G>A	ENSP00000359652.4:p.Gly2085=
ENST00000370621.7:c.6255G>A	ENSP00000359655.3:p.Gly2085=
ENST00000503581.5:c.6255G>A	ENSP00000424243.1:p.Gly2085=
NM_001142800.1:c.6255G>A	NP_001136272.1:p.Gly2085=
NM_001292009.1:c.6255G>A	NP_001278938.1:p.Gly2085=
NM_001142800.2:c.6255G>A MANE Select	NP_001136272.1:p.Gly2085=
NM_001292009.2:c.6255G>A	NP_001278938.1:p.Gly2085=