Canonical Allele Identifier: CA347304441
Gene: ACTG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.74141965T>A (hg19) chr2:g.73914838T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.73914838T>A , CM000664.2:g.73914838T>A GRCh38
NC_000002.11:g.74141965T>A , CM000664.1:g.74141965T>A GRCh37
NC_000002.10:g.73995473T>A NCBI36
NG_034140.1:g.26873T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000345517.8:c.772T>A MANE Select ENSP00000295137.3:p.Cys258Ser
ENST00000345517.7:c.772T>A ENSP00000295137.3:p.Cys258Ser
ENST00000409624.1:c.772T>A ENSP00000386857.1:p.Cys258Ser
ENST00000409731.7:c.643T>A ENSP00000386929.3:p.Cys215Ser
ENST00000438902.6:c.*837T>A ENSP00000410706.2:n.*837T>A
NM_001199893.1:c.643T>A NP_001186822.1:p.Cys215Ser
NM_001615.3:c.772T>A NP_001606.1:p.Cys258Ser
NM_001199893.2:c.643T>A NP_001186822.1:p.Cys215Ser
NM_001615.4:c.772T>A MANE Select NP_001606.1:p.Cys258Ser
Search 100 bp 5'
Search 100 bp 3'