Canonical Allele Identifier: CA338622391
Gene: EPHA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.16458641T>G (hg19) chr1:g.16132146T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132146T>G , CM000663.2:g.16132146T>G GRCh38
NC_000001.10:g.16458641T>G , CM000663.1:g.16458641T>G GRCh37
NC_000001.9:g.16331228T>G NCBI36
NG_021396.1:g.28942A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000358432.8:c.2243A>C MANE Select ENSP00000351209.5:p.Asn748Thr
ENST00000358432.7:c.2243A>C ENSP00000351209.5:p.Asn748Thr
NM_004431.3:c.2243A>C NP_004422.2:p.Asn748Thr
NM_001329090.1:c.2081A>C NP_001316019.1:p.Asn694Thr
NM_004431.4:c.2243A>C NP_004422.2:p.Asn748Thr
NM_004431.5:c.2243A>C MANE Select NP_004422.2:p.Asn748Thr
NM_001329090.2:c.2081A>C NP_001316019.1:p.Asn694Thr
Search 100 bp 5'
Search 100 bp 3'