Canonical Allele Identifier: CA2695493495
Gene: EPHA2 HGNC NCBI

Linked Data

dbSNP Id: rs2124200126
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132043A>G , CM000663.2:g.16132043A>G GRCh38
NC_000001.10:g.16458538A>G , CM000663.1:g.16458538A>G GRCh37
NC_000001.9:g.16331125A>G NCBI36
NG_021396.1:g.29045T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2325+21T>C MANE Select ENSP00000351209.5:n.2325+21T>C
ENST00000358432.7:c.2325+21T>C ENSP00000351209.5:n.2325+21T>C
NM_004431.3:c.2325+21T>C NP_004422.2:n.2325+21T>C
NM_001329090.1:c.2163+21T>C NP_001316019.1:n.2163+21T>C
NM_004431.4:c.2325+21T>C NP_004422.2:n.2325+21T>C
NM_004431.5:c.2325+21T>C MANE Select NP_004422.2:n.2325+21T>C
NM_001329090.2:c.2163+21T>C NP_001316019.1:n.2163+21T>C
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