Canonical Allele Identifier: CA596310060
Gene: EIF3A HGNC NCBI

Linked Data

dbSNP Id: rs1415046898
gnomAD v2: 10-120810029-G-T
gnomAD v4: 10-119050517-G-T
MyVariant Identifiers: chr10:g.120810029G>T (hg19) chr10:g.119050517G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050517G>T , CM000672.2:g.119050517G>T GRCh38
NC_000010.10:g.120810029G>T , CM000672.1:g.120810029G>T GRCh37
NC_000010.9:g.120800019G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369144.8:c.2473+4C>A MANE Select ENSP00000358140.3:n.2473+4C>A
ENST00000369144.7:c.2473+4C>A ENSP00000358140.3:n.2473+4C>A
ENST00000541549.2:c.2473+4C>A ENSP00000438178.2:n.2473+4C>A
NM_003750.2:c.2473+4C>A NP_003741.1:n.2473+4C>A
NM_003750.3:c.2473+4C>A NP_003741.1:n.2473+4C>A
NM_003750.4:c.2473+4C>A MANE Select NP_003741.1:n.2473+4C>A
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