Canonical Allele Identifier: CA364384875

Gene: EYS

Linked Data

• dbSNP Id: rs1284011398
• gnomAD v3: 6-63788143-A-C
• gnomAD v4: 6-63788143-A-C
• MyVariant Identifiers: chr6:g.64498036A>C (hg19) ; chr6:g.63788143A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788143A>C , CM000668.2:g.63788143A>C	GRCh38
NC_000006.11:g.64498036A>C , CM000668.1:g.64498036A>C	GRCh37
NC_000006.10:g.64555995A>C	NCBI36
NG_023443.1:g.1924083T>G
NG_023443.2:g.1924083T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7685T>G MANE Select	ENSP00000424243.1:p.Leu2562Arg
ENST00000370616.6:c.7685T>G	ENSP00000359650.2:p.Leu2562Arg
ENST00000370618.7:c.7685T>G	ENSP00000359652.4:p.Leu2562Arg
ENST00000370621.7:c.7685T>G	ENSP00000359655.3:p.Leu2562Arg
ENST00000398580.3:c.999T>G
ENST00000486069.1:n.325T>G
ENST00000503581.5:c.7685T>G	ENSP00000424243.1:p.Leu2562Arg
NM_001142800.1:c.7685T>G	NP_001136272.1:p.Leu2562Arg
NM_001292009.1:c.7685T>G	NP_001278938.1:p.Leu2562Arg
NM_001142800.2:c.7685T>G MANE Select	NP_001136272.1:p.Leu2562Arg
NM_001292009.2:c.7685T>G	NP_001278938.1:p.Leu2562Arg