Canonical Allele Identifier: CA1089794980

Gene: EYS

Linked Data

• dbSNP Id: rs1770422503
• gnomAD v3: 6-63788380-C-T
• gnomAD v4: 6-63788380-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788380C>T , CM000668.2:g.63788380C>T	GRCh38
NC_000006.11:g.64498273C>T , CM000668.1:g.64498273C>T	GRCh37
NC_000006.10:g.64556232C>T	NCBI36
NG_023443.1:g.1923846G>A
NG_023443.2:g.1923846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7579-131G>A MANE Select	ENSP00000424243.1:n.7579-131G>A
ENST00000370616.6:c.7579-131G>A	ENSP00000359650.2:n.7579-131G>A
ENST00000370618.7:c.7579-131G>A	ENSP00000359652.4:n.7579-131G>A
ENST00000370621.7:c.7579-131G>A	ENSP00000359655.3:n.7579-131G>A
ENST00000398580.3:c.893-131G>A
ENST00000486069.1:n.219-131G>A
ENST00000503581.5:c.7579-131G>A	ENSP00000424243.1:n.7579-131G>A
NM_001142800.1:c.7579-131G>A	NP_001136272.1:n.7579-131G>A
NM_001292009.1:c.7579-131G>A	NP_001278938.1:n.7579-131G>A
NM_001142800.2:c.7579-131G>A MANE Select	NP_001136272.1:n.7579-131G>A
NM_001292009.2:c.7579-131G>A	NP_001278938.1:n.7579-131G>A