Canonical Allele Identifier: CA50423482

Gene: ACTG2

Linked Data

• dbSNP Id: rs867923618
• MyVariant Identifiers: chr2:g.74141975C>T (hg19) ; chr2:g.73914848C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914848C>T , CM000664.2:g.73914848C>T	GRCh38
NC_000002.11:g.74141975C>T , CM000664.1:g.74141975C>T	GRCh37
NC_000002.10:g.73995483C>T	NCBI36
NG_034140.1:g.26883C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000345517.8:c.782C>T MANE Select	ENSP00000295137.3:p.Thr261Ile
ENST00000345517.7:c.782C>T	ENSP00000295137.3:p.Thr261Ile
ENST00000409624.1:c.782C>T	ENSP00000386857.1:p.Thr261Ile
ENST00000409731.7:c.653C>T	ENSP00000386929.3:p.Thr218Ile
ENST00000438902.6:c.*847C>T	ENSP00000410706.2:n.*847C>T
NM_001199893.1:c.653C>T	NP_001186822.1:p.Thr218Ile
NM_001615.3:c.782C>T	NP_001606.1:p.Thr261Ile
NM_001199893.2:c.653C>T	NP_001186822.1:p.Thr218Ile
NM_001615.4:c.782C>T MANE Select	NP_001606.1:p.Thr261Ile