Canonical Allele Identifier: CA122982
Gene: EPHA2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13262
dbSNP Id: rs116506614

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132227C>T , CM000663.2:g.16132227C>T GRCh38
NC_000001.9:g.16331309C>T NCBI36
NC_000001.10:g.16458722C>T , CM000663.1:g.16458722C>T GRCh37
NG_021396.1:g.28861G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358432.7:c.2162G>A ENSP00000351209.5:p.Arg721Gln
NM_004431.3:c.2162G>A VV NP_004422.2:p.Arg721Gln