Canonical Allele Identifier: CA625513
Gene: EPHA2 HGNC NCBI

Linked Data

dbSNP Id: rs113882203
gnomAD v2: 1-16475220-C-T
gnomAD v3: 1-16148725-C-T
gnomAD v4: 1-16148725-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16148725C>T , CM000663.2:g.16148725C>T GRCh38
NC_000001.10:g.16475220C>T , CM000663.1:g.16475220C>T GRCh37
NC_000001.9:g.16347807C>T NCBI36
NG_021396.1:g.12363G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358432.8:c.476G>A MANE Select ENSP00000351209.5:p.Arg159His
ENST00000358432.7:c.476G>A ENSP00000351209.5:p.Arg159His
ENST00000461614.1:n.528G>A
NM_004431.3:c.476G>A NP_004422.2:p.Arg159His
NM_001329090.1:c.314G>A NP_001316019.1:p.Arg105His
NM_004431.4:c.476G>A NP_004422.2:p.Arg159His
XM_017000537.1:c.476G>A XP_016856026.1:p.Arg159His
NM_004431.5:c.476G>A MANE Select NP_004422.2:p.Arg159His
NM_001329090.2:c.314G>A NP_001316019.1:p.Arg105His