Canonical Allele Identifier: CA347304464

Gene: ACTG2

Linked Data

• MyVariant Identifiers: chr2:g.74141974A>G (hg19) ; chr2:g.73914847A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914847A>G , CM000664.2:g.73914847A>G	GRCh38
NC_000002.11:g.74141974A>G , CM000664.1:g.74141974A>G	GRCh37
NC_000002.10:g.73995482A>G	NCBI36
NG_034140.1:g.26882A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000345517.8:c.781A>G MANE Select	ENSP00000295137.3:p.Thr261Ala
ENST00000345517.7:c.781A>G	ENSP00000295137.3:p.Thr261Ala
ENST00000409624.1:c.781A>G	ENSP00000386857.1:p.Thr261Ala
ENST00000409731.7:c.652A>G	ENSP00000386929.3:p.Thr218Ala
ENST00000438902.6:c.*846A>G	ENSP00000410706.2:n.*846A>G
NM_001199893.1:c.652A>G	NP_001186822.1:p.Thr218Ala
NM_001615.3:c.781A>G	NP_001606.1:p.Thr261Ala
NM_001199893.2:c.652A>G	NP_001186822.1:p.Thr218Ala
NM_001615.4:c.781A>G MANE Select	NP_001606.1:p.Thr261Ala