Canonical Allele Identifier: CA471628847
Gene: EIF3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.120810082T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050570T>C , CM000672.2:g.119050570T>C GRCh38
NC_000010.10:g.120810082T>C , CM000672.1:g.120810082T>C GRCh37
NC_000010.9:g.120800072T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2424A>G MANE Select ENSP00000358140.3:p.Arg808=
ENST00000369144.7:c.2424A>G ENSP00000358140.3:p.Arg808=
ENST00000541549.2:c.2424A>G ENSP00000438178.2:p.Arg808=
NM_003750.2:c.2424A>G NP_003741.1:p.Arg808=
NM_003750.3:c.2424A>G NP_003741.1:p.Arg808=
NM_003750.4:c.2424A>G MANE Select NP_003741.1:p.Arg808=
Search 100 bp 5'
Search 100 bp 3'