Canonical Allele Identifier: CA4147127

Gene: ACTB

Linked Data

• dbSNP Id: rs750565033
• ExAC: 7:5568957 G / C
• gnomAD v2: 7-5568957-G-C
• gnomAD v4: 7-5529326-G-C
• MyVariant Identifiers: chr7:g.5568957G>C (hg19) ; chr7:g.5529326G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529326G>C , CM000669.2:g.5529326G>C	GRCh38
NC_000007.13:g.5568957G>C , CM000669.1:g.5568957G>C	GRCh37
NC_000007.12:g.5535483G>C	NCBI36
NG_007992.1:g.6276C>G , LRG_132:g.6276C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.198C>G	ENSP00000399487.2:p.Thr66=
ENST00000432588.6:c.198C>G	ENSP00000407473.2:p.Thr66=
ENST00000473257.3:c.69C>G	ENSP00000501773.1:p.Thr23=
ENST00000477812.2:n.405C>G
ENST00000484841.6:n.352C>G
ENST00000493945.6:c.198C>G	ENSP00000494269.1:p.Thr66=
ENST00000642480.2:c.198C>G	ENSP00000495995.2:p.Thr66=
ENST00000645025.1:n.281C>G
ENST00000645576.1:c.198C>G	ENSP00000496101.1:p.Thr66=
ENST00000646664.1:c.198C>G MANE Select	ENSP00000494750.1:p.Thr66=
ENST00000647275.1:c.-3-607C>G	ENSP00000494185.1:n.-3-607C>G
ENST00000674681.1:c.198C>G	ENSP00000502821.1:p.Thr66=
ENST00000675515.1:c.198C>G	ENSP00000501862.1:p.Thr66=
ENST00000676189.1:c.198C>G	ENSP00000502538.1:p.Thr66=
ENST00000676319.1:c.87+245C>G	ENSP00000502193.1:n.87+245C>G
ENST00000676397.1:c.198C>G	ENSP00000502286.1:p.Thr66=
ENST00000331789.9:c.198C>G	ENSP00000349960.4:p.Thr66=
ENST00000414620.1:c.198C>G	ENSP00000401032.1:p.Thr66=
ENST00000417101.1:c.207C>G	ENSP00000399487.1:p.Thr69=
ENST00000425660.5:c.198C>G	ENSP00000409264.1:p.Thr66=
ENST00000432588.5:c.198C>G	ENSP00000407473.1:p.Thr66=
ENST00000443528.5:c.198C>G	ENSP00000393951.1:p.Thr66=
ENST00000462494.5:n.282C>G
ENST00000473257.1:n.82-607C>G
ENST00000477812.1:n.405C>G
ENST00000480301.1:n.398C>G
ENST00000484841.5:n.353C>G
ENST00000493945.5:n.204C>G
NM_001101.3:c.198C>G , LRG_132t1:c.198C>G	NP_001092.1:p.Thr66=
NM_001101.4:c.198C>G	NP_001092.1:p.Thr66=
NM_001101.5:c.198C>G MANE Select	NP_001092.1:p.Thr66=