Canonical Allele Identifier: CA4147141
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 698769
dbSNP Id: rs199651295
gnomAD v2: 7-5569038-A-T
gnomAD v3: 7-5529407-A-T
gnomAD v4: 7-5529407-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529407A>T , CM000669.2:g.5529407A>T GRCh38
NC_000007.13:g.5569038A>T , CM000669.1:g.5569038A>T GRCh37
NC_000007.12:g.5535564A>T NCBI36
NG_007992.1:g.6195T>A , LRG_132:g.6195T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.124-7T>A ENSP00000399487.2:n.124-7T>A
ENST00000432588.6:c.124-7T>A ENSP00000407473.2:n.124-7T>A
ENST00000473257.3:c.-6-7T>A ENSP00000501773.1:n.-6-7T>A
ENST00000477812.2:n.324T>A
ENST00000484841.6:n.278-7T>A
ENST00000493945.6:c.124-7T>A ENSP00000494269.1:n.124-7T>A
ENST00000642480.2:c.124-7T>A ENSP00000495995.2:n.124-7T>A
ENST00000645025.1:n.207-7T>A
ENST00000645576.1:c.124-7T>A ENSP00000496101.1:n.124-7T>A
ENST00000646664.1:c.124-7T>A MANE Select ENSP00000494750.1:n.124-7T>A
ENST00000647275.1:c.-3-688T>A ENSP00000494185.1:n.-3-688T>A
ENST00000674681.1:c.124-7T>A ENSP00000502821.1:n.124-7T>A
ENST00000675515.1:c.124-7T>A ENSP00000501862.1:n.124-7T>A
ENST00000676189.1:c.124-7T>A ENSP00000502538.1:n.124-7T>A
ENST00000676319.1:c.87+164T>A ENSP00000502193.1:n.87+164T>A
ENST00000676397.1:c.124-7T>A ENSP00000502286.1:n.124-7T>A
ENST00000331789.9:c.124-7T>A ENSP00000349960.4:n.124-7T>A
ENST00000414620.1:c.124-7T>A ENSP00000401032.1:n.124-7T>A
ENST00000417101.1:c.133-7T>A ENSP00000399487.1:n.133-7T>A
ENST00000425660.5:c.124-7T>A ENSP00000409264.1:n.124-7T>A
ENST00000432588.5:c.124-7T>A ENSP00000407473.1:n.124-7T>A
ENST00000443528.5:c.124-7T>A ENSP00000393951.1:n.124-7T>A
ENST00000462494.5:n.208-7T>A
ENST00000473257.1:n.82-688T>A
ENST00000477812.1:n.324T>A
ENST00000480301.1:n.317T>A
ENST00000484841.5:n.279-7T>A
ENST00000493945.5:n.130-7T>A
NM_001101.3:c.124-7T>A , LRG_132t1:c.124-7T>A NP_001092.1:n.124-7T>A
NM_001101.4:c.124-7T>A NP_001092.1:n.124-7T>A
NM_001101.5:c.124-7T>A MANE Select NP_001092.1:n.124-7T>A