Canonical Allele Identifier: CA213216
Gene: ACTB HGNC NCBI

Linked Data

ClinVar Variation Id: 127167
ClinVar RCV Id: RCV000133570 RCV003238727
dbSNP Id: rs587779773
MyVariant Identifiers: chr7:g.5568799A>G (hg19) chr7:g.5529168A>G (hg38)
PubMed: PMID:25052316
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.5529168A>G , CM000669.2:g.5529168A>G GRCh38
NC_000007.13:g.5568799A>G , CM000669.1:g.5568799A>G GRCh37
NC_000007.12:g.5535325A>G NCBI36
NG_007992.1:g.6434T>C , LRG_132:g.6434T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000432588.6:c.356T>C ENSP00000407473.2:p.Met119Thr
ENST00000473257.3:c.227T>C ENSP00000501773.1:p.Met76Thr
ENST00000477812.2:n.563T>C
ENST00000484841.6:n.510T>C
ENST00000493945.6:c.356T>C ENSP00000494269.1:p.Met119Thr
ENST00000642480.2:c.356T>C ENSP00000495995.2:p.Met119Thr
ENST00000645025.1:n.439T>C
ENST00000645576.1:c.356T>C ENSP00000496101.1:p.Met119Thr
ENST00000646664.1:c.356T>C MANE Select ENSP00000494750.1:p.Met119Thr
ENST00000647275.1:c.-3-449T>C ENSP00000494185.1:n.-3-449T>C
ENST00000674681.1:c.356T>C ENSP00000502821.1:p.Met119Thr
ENST00000675515.1:c.356T>C ENSP00000501862.1:p.Met119Thr
ENST00000676189.1:c.356T>C ENSP00000502538.1:p.Met119Thr
ENST00000676319.1:c.87+403T>C ENSP00000502193.1:n.87+403T>C
ENST00000676397.1:c.356T>C ENSP00000502286.1:p.Met119Thr
ENST00000331789.9:c.356T>C ENSP00000349960.4:p.Met119Thr
ENST00000425660.5:c.356T>C ENSP00000409264.1:p.Met119Thr
ENST00000432588.5:c.356T>C ENSP00000407473.1:p.Met119Thr
ENST00000462494.5:n.440T>C
ENST00000473257.1:n.82-449T>C
ENST00000477812.1:n.563T>C
ENST00000480301.1:n.556T>C
ENST00000484841.5:n.511T>C
ENST00000493945.5:n.362T>C
NM_001101.3:c.356T>C , LRG_132t1:c.356T>C NP_001092.1:p.Met119Thr
XM_006715764.1:c.-351T>C XP_006715827.1:n.-351T>C
NM_001101.4:c.356T>C NP_001092.1:p.Met119Thr
NM_001101.5:c.356T>C MANE Select NP_001092.1:p.Met119Thr
Search 100 bp 5'
Search 100 bp 3'