Canonical Allele Identifier: CA471628848
Gene: EIF3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.120810084T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050572T>G , CM000672.2:g.119050572T>G GRCh38
NC_000010.10:g.120810084T>G , CM000672.1:g.120810084T>G GRCh37
NC_000010.9:g.120800074T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2422A>C MANE Select ENSP00000358140.3:p.Arg808=
ENST00000369144.7:c.2422A>C ENSP00000358140.3:p.Arg808=
ENST00000541549.2:c.2422A>C ENSP00000438178.2:p.Arg808=
NM_003750.2:c.2422A>C NP_003741.1:p.Arg808=
NM_003750.3:c.2422A>C NP_003741.1:p.Arg808=
NM_003750.4:c.2422A>C MANE Select NP_003741.1:p.Arg808=
Search 100 bp 5'
Search 100 bp 3'