Canonical Allele Identifier: CA450758757
Gene: EYS HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.64940504A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.64230611A>C , CM000668.2:g.64230611A>C GRCh38
NC_000006.11:g.64940504A>C , CM000668.1:g.64940504A>C GRCh37
NC_000006.10:g.64998463A>C NCBI36
NG_023443.1:g.1481615T>G
NG_023443.2:g.1481615T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.6405T>G MANE Select ENSP00000424243.1:p.Thr2135=
ENST00000370616.6:c.6405T>G ENSP00000359650.2:p.Thr2135=
ENST00000370618.7:c.6405T>G ENSP00000359652.4:p.Thr2135=
ENST00000370621.7:c.6405T>G ENSP00000359655.3:p.Thr2135=
ENST00000503581.5:c.6405T>G ENSP00000424243.1:p.Thr2135=
NM_001142800.1:c.6405T>G NP_001136272.1:p.Thr2135=
NM_001292009.1:c.6405T>G NP_001278938.1:p.Thr2135=
NM_001142800.2:c.6405T>G MANE Select NP_001136272.1:p.Thr2135=
NM_001292009.2:c.6405T>G NP_001278938.1:p.Thr2135=