Canonical Allele Identifier: CA450765810

Gene: EYS

Linked Data

• dbSNP Id: rs1462805735
• gnomAD v2: 6-65767517-A-T
• gnomAD v4: 6-65057624-A-T
• MyVariant Identifiers: chr6:g.65767517A>T (hg19) ; chr6:g.65057624A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.65057624A>T , CM000668.2:g.65057624A>T	GRCh38
NC_000006.11:g.65767517A>T , CM000668.1:g.65767517A>T	GRCh37
NC_000006.10:g.65824238A>T	NCBI36
NG_023443.1:g.654602T>A
NG_023443.2:g.654602T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000503581.6:c.2127T>A MANE Select	ENSP00000424243.1:p.Pro709=
ENST00000370616.6:c.2127T>A	ENSP00000359650.2:p.Pro709=
ENST00000370618.7:c.2127T>A	ENSP00000359652.4:p.Pro709=
ENST00000370621.7:c.2127T>A	ENSP00000359655.3:p.Pro709=
ENST00000503581.5:c.2127T>A	ENSP00000424243.1:p.Pro709=
NM_001142800.1:c.2127T>A	NP_001136272.1:p.Pro709=
NM_001292009.1:c.2127T>A	NP_001278938.1:p.Pro709=
NM_001142800.2:c.2127T>A MANE Select	NP_001136272.1:p.Pro709=
NM_001292009.2:c.2127T>A	NP_001278938.1:p.Pro709=