Canonical Allele Identifier: CA366706542

Gene: ACTB

Linked Data

• MyVariant Identifiers: chr7:g.5569166C>A (hg19) ; chr7:g.5529535C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5529535C>A , CM000669.2:g.5529535C>A	GRCh38
NC_000007.13:g.5569166C>A , CM000669.1:g.5569166C>A	GRCh37
NC_000007.12:g.5535692C>A	NCBI36
NG_007992.1:g.6067G>T , LRG_132:g.6067G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000417101.2:c.123G>T	ENSP00000399487.2:p.Gln41His
ENST00000432588.6:c.123G>T	ENSP00000407473.2:p.Gln41His
ENST00000473257.3:c.-6-135G>T	ENSP00000501773.1:n.-6-135G>T
ENST00000477812.2:n.196G>T
ENST00000484841.6:n.277G>T
ENST00000493945.6:c.123G>T	ENSP00000494269.1:p.Gln41His
ENST00000642480.2:c.123G>T	ENSP00000495995.2:p.Gln41His
ENST00000645025.1:n.206G>T
ENST00000645576.1:c.123G>T	ENSP00000496101.1:p.Gln41His
ENST00000646664.1:c.123G>T MANE Select	ENSP00000494750.1:p.Gln41His
ENST00000647275.1:c.-3-816G>T	ENSP00000494185.1:n.-3-816G>T
ENST00000674681.1:c.123G>T	ENSP00000502821.1:p.Gln41His
ENST00000675515.1:c.123G>T	ENSP00000501862.1:p.Gln41His
ENST00000676189.1:c.123G>T	ENSP00000502538.1:p.Gln41His
ENST00000676319.1:c.87+36G>T	ENSP00000502193.1:n.87+36G>T
ENST00000676397.1:c.123G>T	ENSP00000502286.1:p.Gln41His
ENST00000331789.9:c.123G>T	ENSP00000349960.4:p.Gln41His
ENST00000414620.1:c.123G>T	ENSP00000401032.1:p.Gln41His
ENST00000417101.1:c.132G>T	ENSP00000399487.1:p.Gln44His
ENST00000425660.5:c.123G>T	ENSP00000409264.1:p.Gln41His
ENST00000432588.5:c.123G>T	ENSP00000407473.1:p.Gln41His
ENST00000443528.5:c.123G>T	ENSP00000393951.1:p.Gln41His
ENST00000462494.5:n.207G>T
ENST00000473257.1:n.82-816G>T
ENST00000477812.1:n.196G>T
ENST00000480301.1:n.189G>T
ENST00000484841.5:n.278G>T
ENST00000493945.5:n.129G>T
NM_001101.3:c.123G>T , LRG_132t1:c.123G>T	NP_001092.1:p.Gln41His
NM_001101.4:c.123G>T	NP_001092.1:p.Gln41His
NM_001101.5:c.123G>T MANE Select	NP_001092.1:p.Gln41His