Canonical Allele Identifier: CA624876
Gene: EPHA2 HGNC NCBI

Linked Data

dbSNP Id: rs755197719
ExAC: 1:16458583 G / A
gnomAD v2: 1-16458583-G-A
gnomAD v3: 1-16132088-G-A
gnomAD v4: 1-16132088-G-A
COSMIC: COSM424447
MyVariant Identifiers: chr1:g.16458583G>A (hg19) chr1:g.16132088G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132088G>A , CM000663.2:g.16132088G>A GRCh38
NC_000001.10:g.16458583G>A , CM000663.1:g.16458583G>A GRCh37
NC_000001.9:g.16331170G>A NCBI36
NG_021396.1:g.29000C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2301C>T MANE Select ENSP00000351209.5:p.Asp767=
ENST00000358432.7:c.2301C>T ENSP00000351209.5:p.Asp767=
NM_004431.3:c.2301C>T NP_004422.2:p.Asp767=
NM_001329090.1:c.2139C>T NP_001316019.1:p.Asp713=
NM_004431.4:c.2301C>T NP_004422.2:p.Asp767=
NM_004431.5:c.2301C>T MANE Select NP_004422.2:p.Asp767=
NM_001329090.2:c.2139C>T NP_001316019.1:p.Asp713=
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