Canonical Allele Identifier: CA347304450

Gene: ACTG2

Linked Data

• MyVariant Identifiers: chr2:g.74141968C>G (hg19) ; chr2:g.73914841C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73914841C>G , CM000664.2:g.73914841C>G	GRCh38
NC_000002.11:g.74141968C>G , CM000664.1:g.74141968C>G	GRCh37
NC_000002.10:g.73995476C>G	NCBI36
NG_034140.1:g.26876C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000345517.8:c.775C>G MANE Select	ENSP00000295137.3:p.Pro259Ala
ENST00000345517.7:c.775C>G	ENSP00000295137.3:p.Pro259Ala
ENST00000409624.1:c.775C>G	ENSP00000386857.1:p.Pro259Ala
ENST00000409731.7:c.646C>G	ENSP00000386929.3:p.Pro216Ala
ENST00000438902.6:c.*840C>G	ENSP00000410706.2:n.*840C>G
NM_001199893.1:c.646C>G	NP_001186822.1:p.Pro216Ala
NM_001615.3:c.775C>G	NP_001606.1:p.Pro259Ala
NM_001199893.2:c.646C>G	NP_001186822.1:p.Pro216Ala
NM_001615.4:c.775C>G MANE Select	NP_001606.1:p.Pro259Ala