Canonical Allele Identifier: CA347304447
Gene: ACTG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.74141967C>A (hg19) chr2:g.73914840C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73914840C>A , CM000664.2:g.73914840C>A GRCh38
NC_000002.11:g.74141967C>A , CM000664.1:g.74141967C>A GRCh37
NC_000002.10:g.73995475C>A NCBI36
NG_034140.1:g.26875C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000345517.8:c.774C>A MANE Select ENSP00000295137.3:p.Cys258Ter
ENST00000345517.7:c.774C>A ENSP00000295137.3:p.Cys258Ter
ENST00000409624.1:c.774C>A ENSP00000386857.1:p.Cys258Ter
ENST00000409731.7:c.645C>A ENSP00000386929.3:p.Cys215Ter
ENST00000438902.6:c.*839C>A ENSP00000410706.2:n.*839C>A
NM_001199893.1:c.645C>A NP_001186822.1:p.Cys215Ter
NM_001615.3:c.774C>A NP_001606.1:p.Cys258Ter
NM_001199893.2:c.645C>A NP_001186822.1:p.Cys215Ter
NM_001615.4:c.774C>A MANE Select NP_001606.1:p.Cys258Ter
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