Canonical Allele Identifier: CA347304439

Gene: ACTG2

Linked Data

• MyVariant Identifiers: chr2:g.74141963G>C (hg19) ; chr2:g.73914836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914836G>C , CM000664.2:g.73914836G>C	GRCh38
NC_000002.11:g.74141963G>C , CM000664.1:g.74141963G>C	GRCh37
NC_000002.10:g.73995471G>C	NCBI36
NG_034140.1:g.26871G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.770G>C MANE Select	ENSP00000295137.3:p.Arg257Pro
ENST00000345517.7:c.770G>C	ENSP00000295137.3:p.Arg257Pro
ENST00000409624.1:c.770G>C	ENSP00000386857.1:p.Arg257Pro
ENST00000409731.7:c.641G>C	ENSP00000386929.3:p.Arg214Pro
ENST00000438902.6:c.*835G>C	ENSP00000410706.2:n.*835G>C
NM_001199893.1:c.641G>C	NP_001186822.1:p.Arg214Pro
NM_001615.3:c.770G>C	NP_001606.1:p.Arg257Pro
NM_001199893.2:c.641G>C	NP_001186822.1:p.Arg214Pro
NM_001615.4:c.770G>C MANE Select	NP_001606.1:p.Arg257Pro