Canonical Allele Identifier: CA153195651

Gene: ACTB

Linked Data

• dbSNP Id: rs907481916
• gnomAD v2: 7-5568526-A-T
• gnomAD v3: 7-5528895-A-T
• gnomAD v4: 7-5528895-A-T
• MyVariant Identifiers: chr7:g.5568526A>T (hg19) ; chr7:g.5528895A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5528895A>T , CM000669.2:g.5528895A>T	GRCh38
NC_000007.13:g.5568526A>T , CM000669.1:g.5568526A>T	GRCh37
NC_000007.12:g.5535052A>T	NCBI36
NG_007992.1:g.6707T>A , LRG_132:g.6707T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432588.6:c.364-176T>A	ENSP00000407473.2:n.364-176T>A
ENST00000473257.3:c.235-176T>A	ENSP00000501773.1:n.235-176T>A
ENST00000477812.2:n.735T>A
ENST00000484841.6:n.558+124T>A
ENST00000493945.6:c.364-176T>A	ENSP00000494269.1:n.364-176T>A
ENST00000642480.2:c.364-176T>A	ENSP00000495995.2:n.364-176T>A
ENST00000645576.1:c.364-224T>A	ENSP00000496101.1:n.364-224T>A
ENST00000646664.1:c.364-176T>A MANE Select	ENSP00000494750.1:n.364-176T>A
ENST00000647275.1:c.-3-176T>A	ENSP00000494185.1:n.-3-176T>A
ENST00000674681.1:c.364-176T>A	ENSP00000502821.1:n.364-176T>A
ENST00000675515.1:c.364-176T>A	ENSP00000501862.1:n.364-176T>A
ENST00000676189.1:c.375-188T>A	ENSP00000502538.1:n.375-188T>A
ENST00000676319.1:c.87+676T>A	ENSP00000502193.1:n.87+676T>A
ENST00000676397.1:c.364-176T>A	ENSP00000502286.1:n.364-176T>A
ENST00000331789.9:c.364-176T>A	ENSP00000349960.4:n.364-176T>A
ENST00000425660.5:c.*26+124T>A	ENSP00000409264.1:n.*26+124T>A
ENST00000432588.5:c.364-176T>A	ENSP00000407473.1:n.364-176T>A
ENST00000462494.5:n.713T>A
ENST00000473257.1:n.82-176T>A
ENST00000477812.1:n.571-176T>A
ENST00000484841.5:n.519-176T>A
ENST00000493945.5:n.370-176T>A
NM_001101.3:c.364-176T>A , LRG_132t1:c.364-176T>A	NP_001092.1:n.364-176T>A
XM_006715764.1:c.-179T>A	XP_006715827.1:n.-179T>A
NM_001101.4:c.364-176T>A	NP_001092.1:n.364-176T>A
NM_001101.5:c.364-176T>A MANE Select	NP_001092.1:n.364-176T>A