Canonical Allele Identifier: CA347304458

Gene: ACTG2

Linked Data

• MyVariant Identifiers: chr2:g.74141972A>T (hg19) ; chr2:g.73914845A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914845A>T , CM000664.2:g.73914845A>T	GRCh38
NC_000002.11:g.74141972A>T , CM000664.1:g.74141972A>T	GRCh37
NC_000002.10:g.73995480A>T	NCBI36
NG_034140.1:g.26880A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.779A>T MANE Select	ENSP00000295137.3:p.Glu260Val
ENST00000345517.7:c.779A>T	ENSP00000295137.3:p.Glu260Val
ENST00000409624.1:c.779A>T	ENSP00000386857.1:p.Glu260Val
ENST00000409731.7:c.650A>T	ENSP00000386929.3:p.Glu217Val
ENST00000438902.6:c.*844A>T	ENSP00000410706.2:n.*844A>T
NM_001199893.1:c.650A>T	NP_001186822.1:p.Glu217Val
NM_001615.3:c.779A>T	NP_001606.1:p.Glu260Val
NM_001199893.2:c.650A>T	NP_001186822.1:p.Glu217Val
NM_001615.4:c.779A>T MANE Select	NP_001606.1:p.Glu260Val