Canonical Allele Identifier: CA140242860

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.63778093C>T , CM000668.2:g.63778093C>T GRCh38
NC_000006.11:g.64487986C>T , CM000668.1:g.64487986C>T GRCh37
NC_000006.10:g.64545945C>T NCBI36
NG_023443.1:g.1934133G>A
NG_023443.2:g.1934133G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001142800.2:c.7811G>A (EYS) MANE Select NP_001136272.1:p.Arg2604His
ENST00000503581.6:c.7811G>A (EYS) MANE Select ENSP00000424243.1:p.Arg2604His
NM_001142800.1:c.7811G>A (EYS) NP_001136272.1:p.Arg2604His
NM_001292009.1:c.7811G>A (EYS) NP_001278938.1:p.Arg2604His
NM_001292009.2:c.7811G>A (EYS) NP_001278938.1:p.Arg2604His
ENST00000370616.6:c.7811G>A (EYS) ENSP00000359650.2:p.Arg2604His
ENST00000370618.7:c.7811G>A (EYS) ENSP00000359652.4:p.Arg2604His
ENST00000370621.7:c.7811G>A (EYS) ENSP00000359655.3:p.Arg2604His
ENST00000398580.3:c.1125G>A (EYS)
ENST00000420043.1:n.489C>T (PHF3)
ENST00000503581.5:c.7811G>A (EYS) ENSP00000424243.1:p.Arg2604His
ENST00000505138.1:c.391C>T (PHF3)