Canonical Allele Identifier: CA347304467
Gene: ACTG2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000345517.8:c.782C>G MANE Select ENSP00000295137.3:p.Thr261Ser
ENST00000345517.7:c.782C>G ENSP00000295137.3:p.Thr261Ser
ENST00000409624.1:c.782C>G ENSP00000386857.1:p.Thr261Ser
ENST00000409731.7:c.653C>G ENSP00000386929.3:p.Thr218Ser
ENST00000438902.6:c.*847C>G ENSP00000410706.2:n.*847C>G
NM_001199893.1:c.653C>G NP_001186822.1:p.Thr218Ser
NM_001615.3:c.782C>G NP_001606.1:p.Thr261Ser
NM_001199893.2:c.653C>G NP_001186822.1:p.Thr218Ser
NM_001615.4:c.782C>G MANE Select NP_001606.1:p.Thr261Ser