Canonical Allele Identifier: CA567712392

Gene: EYS

Linked Data

• dbSNP Id: rs1440707923
• gnomAD v2: 6-64791700-G-T
• gnomAD v4: 6-64081807-G-T
• MyVariant Identifiers: chr6:g.64791700G>T (hg19) ; chr6:g.64081807G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.64081807G>T , CM000668.2:g.64081807G>T	GRCh38
NC_000006.11:g.64791700G>T , CM000668.1:g.64791700G>T	GRCh37
NC_000006.10:g.64849659G>T	NCBI36
NG_023443.1:g.1630419C>A
NG_023443.2:g.1630419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503581.6:c.6571+49C>A MANE Select	ENSP00000424243.1:n.6571+49C>A
ENST00000370616.6:c.6571+49C>A	ENSP00000359650.2:n.6571+49C>A
ENST00000370618.7:c.6571+49C>A	ENSP00000359652.4:n.6571+49C>A
ENST00000370621.7:c.6571+49C>A	ENSP00000359655.3:n.6571+49C>A
ENST00000503581.5:c.6571+49C>A	ENSP00000424243.1:n.6571+49C>A
NM_001142800.1:c.6571+49C>A	NP_001136272.1:n.6571+49C>A
NM_001292009.1:c.6571+49C>A	NP_001278938.1:n.6571+49C>A
NM_001142800.2:c.6571+49C>A MANE Select	NP_001136272.1:n.6571+49C>A
NM_001292009.2:c.6571+49C>A	NP_001278938.1:n.6571+49C>A