Canonical Allele Identifier: CA364385409

Gene: EYS

Linked Data

• ClinVar Variation Id: 1696175
• ClinVar RCV Id: RCV002266319
• dbSNP Id: rs2149670380
• MyVariant Identifiers: chr6:g.64498097C>A (hg19) ; chr6:g.63788204C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63788204C>A , CM000668.2:g.63788204C>A	GRCh38
NC_000006.11:g.64498097C>A , CM000668.1:g.64498097C>A	GRCh37
NC_000006.10:g.64556056C>A	NCBI36
NG_023443.1:g.1924022G>T
NG_023443.2:g.1924022G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.7624G>T MANE Select	ENSP00000424243.1:p.Val2542Phe
ENST00000370616.6:c.7624G>T	ENSP00000359650.2:p.Val2542Phe
ENST00000370618.7:c.7624G>T	ENSP00000359652.4:p.Val2542Phe
ENST00000370621.7:c.7624G>T	ENSP00000359655.3:p.Val2542Phe
ENST00000398580.3:c.938G>T
ENST00000486069.1:n.264G>T
ENST00000503581.5:c.7624G>T	ENSP00000424243.1:p.Val2542Phe
NM_001142800.1:c.7624G>T	NP_001136272.1:p.Val2542Phe
NM_001292009.1:c.7624G>T	NP_001278938.1:p.Val2542Phe
NM_001142800.2:c.7624G>T MANE Select	NP_001136272.1:p.Val2542Phe
NM_001292009.2:c.7624G>T	NP_001278938.1:p.Val2542Phe