Canonical Allele Identifier: CA153195688
Gene: ACTB HGNC NCBI

Linked Data

dbSNP Id: rs142116324
gnomAD v4: 7-5529368-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529368G>T , CM000669.2:g.5529368G>T GRCh38
NC_000007.13:g.5568999G>T , CM000669.1:g.5568999G>T GRCh37
NC_000007.12:g.5535525G>T NCBI36
NG_007992.1:g.6234C>A , LRG_132:g.6234C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000417101.2:c.156C>A ENSP00000399487.2:p.Ser52=
ENST00000432588.6:c.156C>A ENSP00000407473.2:p.Ser52=
ENST00000473257.3:c.27C>A ENSP00000501773.1:p.Ser9=
ENST00000477812.2:n.363C>A
ENST00000484841.6:n.310C>A
ENST00000493945.6:c.156C>A ENSP00000494269.1:p.Ser52=
ENST00000642480.2:c.156C>A ENSP00000495995.2:p.Ser52=
ENST00000645025.1:n.239C>A
ENST00000645576.1:c.156C>A ENSP00000496101.1:p.Ser52=
ENST00000646664.1:c.156C>A MANE Select ENSP00000494750.1:p.Ser52=
ENST00000647275.1:c.-3-649C>A ENSP00000494185.1:n.-3-649C>A
ENST00000674681.1:c.156C>A ENSP00000502821.1:p.Ser52=
ENST00000675515.1:c.156C>A ENSP00000501862.1:p.Ser52=
ENST00000676189.1:c.156C>A ENSP00000502538.1:p.Ser52=
ENST00000676319.1:c.87+203C>A ENSP00000502193.1:n.87+203C>A
ENST00000676397.1:c.156C>A ENSP00000502286.1:p.Ser52=
ENST00000331789.9:c.156C>A ENSP00000349960.4:p.Ser52=
ENST00000414620.1:c.156C>A ENSP00000401032.1:p.Ser52=
ENST00000417101.1:c.165C>A ENSP00000399487.1:p.Ser55=
ENST00000425660.5:c.156C>A ENSP00000409264.1:p.Ser52=
ENST00000432588.5:c.156C>A ENSP00000407473.1:p.Ser52=
ENST00000443528.5:c.156C>A ENSP00000393951.1:p.Ser52=
ENST00000462494.5:n.240C>A
ENST00000473257.1:n.82-649C>A
ENST00000477812.1:n.363C>A
ENST00000480301.1:n.356C>A
ENST00000484841.5:n.311C>A
ENST00000493945.5:n.162C>A
NM_001101.3:c.156C>A , LRG_132t1:c.156C>A NP_001092.1:p.Ser52=
NM_001101.4:c.156C>A NP_001092.1:p.Ser52=
NM_001101.5:c.156C>A MANE Select NP_001092.1:p.Ser52=