Canonical Allele Identifier: CA636614377
Gene: EEF1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1568997480
MyVariant Identifiers: chr20:g.62127437G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63496084G>A , CM000682.2:g.63496084G>A GRCh38
NC_000020.10:g.62127437G>A , CM000682.1:g.62127437G>A GRCh37
NC_000020.9:g.61597881G>A NCBI36
NG_034083.1:g.8232C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706948.1:c.145-49C>T ENSP00000516668.1:n.145-49C>T
ENST00000706949.1:c.145-49C>T ENSP00000516669.1:n.145-49C>T
ENST00000217182.6:c.145-49C>T MANE Select ENSP00000217182.3:n.145-49C>T
ENST00000298049.12:c.145-49C>T ENSP00000298049.8:n.145-49C>T
ENST00000642899.1:c.145-49C>T ENSP00000493767.1:n.145-49C>T
ENST00000645357.1:c.145-49C>T ENSP00000494971.1:n.145-49C>T
ENST00000645586.1:n.2665C>T
ENST00000646335.1:c.145-49C>T ENSP00000494752.1:n.145-49C>T
ENST00000675519.1:c.148C>T ENSP00000501859.1:p.Leu50Phe
ENST00000217182.4:c.145-49C>T ENSP00000217182.3:n.145-49C>T
ENST00000298049.11:c.145-49C>T ENSP00000298049.7:n.145-49C>T
NM_001958.3:c.145-49C>T NP_001949.1:n.145-49C>T
NM_001958.4:c.145-49C>T NP_001949.1:n.145-49C>T
NM_001958.5:c.145-49C>T MANE Select NP_001949.1:n.145-49C>T