Canonical Allele Identifier: CA338622292
Gene: EPHA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.16458596A>C (hg19) chr1:g.16132101A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132101A>C , CM000663.2:g.16132101A>C GRCh38
NC_000001.10:g.16458596A>C , CM000663.1:g.16458596A>C GRCh37
NC_000001.9:g.16331183A>C NCBI36
NG_021396.1:g.28987T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2288T>G MANE Select ENSP00000351209.5:p.Val763Gly
ENST00000358432.7:c.2288T>G ENSP00000351209.5:p.Val763Gly
NM_004431.3:c.2288T>G NP_004422.2:p.Val763Gly
NM_001329090.1:c.2126T>G NP_001316019.1:p.Val709Gly
NM_004431.4:c.2288T>G NP_004422.2:p.Val763Gly
NM_004431.5:c.2288T>G MANE Select NP_004422.2:p.Val763Gly
NM_001329090.2:c.2126T>G NP_001316019.1:p.Val709Gly
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