Canonical Allele Identifier: CA4147120
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 1102536
ClinVar RCV Id: RCV001425880
dbSNP Id: rs371726724
gnomAD v2: 7-5568900-G-A
gnomAD v3: 7-5529269-G-A
gnomAD v4: 7-5529269-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529269G>A , CM000669.2:g.5529269G>A GRCh38
NC_000007.13:g.5568900G>A , CM000669.1:g.5568900G>A GRCh37
NC_000007.12:g.5535426G>A NCBI36
NG_007992.1:g.6333C>T , LRG_132:g.6333C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.255C>T ENSP00000399487.2:p.Ile85=
ENST00000432588.6:c.255C>T ENSP00000407473.2:p.Ile85=
ENST00000473257.3:c.126C>T ENSP00000501773.1:p.Ile42=
ENST00000477812.2:n.462C>T
ENST00000484841.6:n.409C>T
ENST00000493945.6:c.255C>T ENSP00000494269.1:p.Ile85=
ENST00000642480.2:c.255C>T ENSP00000495995.2:p.Ile85=
ENST00000645025.1:n.338C>T
ENST00000645576.1:c.255C>T ENSP00000496101.1:p.Ile85=
ENST00000646664.1:c.255C>T MANE Select ENSP00000494750.1:p.Ile85=
ENST00000647275.1:c.-3-550C>T ENSP00000494185.1:n.-3-550C>T
ENST00000674681.1:c.255C>T ENSP00000502821.1:p.Ile85=
ENST00000675515.1:c.255C>T ENSP00000501862.1:p.Ile85=
ENST00000676189.1:c.255C>T ENSP00000502538.1:p.Ile85=
ENST00000676319.1:c.87+302C>T ENSP00000502193.1:n.87+302C>T
ENST00000676397.1:c.255C>T ENSP00000502286.1:p.Ile85=
ENST00000331789.9:c.255C>T ENSP00000349960.4:p.Ile85=
ENST00000417101.1:c.264C>T ENSP00000399487.1:p.Ile88=
ENST00000425660.5:c.255C>T ENSP00000409264.1:p.Ile85=
ENST00000432588.5:c.255C>T ENSP00000407473.1:p.Ile85=
ENST00000443528.5:c.255C>T ENSP00000393951.1:p.Ile85=
ENST00000462494.5:n.339C>T
ENST00000473257.1:n.82-550C>T
ENST00000477812.1:n.462C>T
ENST00000480301.1:n.455C>T
ENST00000484841.5:n.410C>T
ENST00000493945.5:n.261C>T
NM_001101.3:c.255C>T , LRG_132t1:c.255C>T NP_001092.1:p.Ile85=
XM_006715764.1:c.-452C>T XP_006715827.1:n.-452C>T
NM_001101.4:c.255C>T NP_001092.1:p.Ile85=
NM_001101.5:c.255C>T MANE Select NP_001092.1:p.Ile85=