Canonical Allele Identifier: CA2679288019
Gene: EYS HGNC NCBI

Linked Data

gnomAD v4: 6-65057548-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.65057548C>A , CM000668.2:g.65057548C>A GRCh38
NC_000006.11:g.65767441C>A , CM000668.1:g.65767441C>A GRCh37
NC_000006.10:g.65824162C>A NCBI36
NG_023443.1:g.654678G>T
NG_023443.2:g.654678G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000503581.6:c.2137+66G>T MANE Select ENSP00000424243.1:n.2137+66G>T
ENST00000370616.6:c.2137+66G>T ENSP00000359650.2:n.2137+66G>T
ENST00000370618.7:c.2137+66G>T ENSP00000359652.4:n.2137+66G>T
ENST00000370621.7:c.2137+66G>T ENSP00000359655.3:n.2137+66G>T
ENST00000503581.5:c.2137+66G>T ENSP00000424243.1:n.2137+66G>T
NM_001142800.1:c.2137+66G>T NP_001136272.1:n.2137+66G>T
NM_001292009.1:c.2137+66G>T NP_001278938.1:n.2137+66G>T
NM_001142800.2:c.2137+66G>T MANE Select NP_001136272.1:n.2137+66G>T
NM_001292009.2:c.2137+66G>T NP_001278938.1:n.2137+66G>T