Canonical Allele Identifier: CA364391447

Gene: EYS

Linked Data

• ClinVar Variation Id: 1482003
• ClinVar RCV Id: RCV002025072
• dbSNP Id: rs2150338023
• MyVariant Identifiers: chr6:g.64940628C>T (hg19) ; chr6:g.64230735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64230735C>T , CM000668.2:g.64230735C>T	GRCh38
NC_000006.11:g.64940628C>T , CM000668.1:g.64940628C>T	GRCh37
NC_000006.10:g.64998587C>T	NCBI36
NG_023443.1:g.1481491G>A
NG_023443.2:g.1481491G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6281G>A MANE Select	ENSP00000424243.1:p.Ser2094Asn
ENST00000370616.6:c.6281G>A	ENSP00000359650.2:p.Ser2094Asn
ENST00000370618.7:c.6281G>A	ENSP00000359652.4:p.Ser2094Asn
ENST00000370621.7:c.6281G>A	ENSP00000359655.3:p.Ser2094Asn
ENST00000503581.5:c.6281G>A	ENSP00000424243.1:p.Ser2094Asn
NM_001142800.1:c.6281G>A	NP_001136272.1:p.Ser2094Asn
NM_001292009.1:c.6281G>A	NP_001278938.1:p.Ser2094Asn
NM_001142800.2:c.6281G>A MANE Select	NP_001136272.1:p.Ser2094Asn
NM_001292009.2:c.6281G>A	NP_001278938.1:p.Ser2094Asn