Canonical Allele Identifier: CA38814488
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs112003167
MyVariant Identifiers: chr1:g.229566995A>T (hg19) chr1:g.229431248A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431248A>T , CM000663.2:g.229431248A>T GRCh38
NC_000001.10:g.229566995A>T , CM000663.1:g.229566995A>T GRCh37
NC_000001.9:g.227633618A>T NCBI36
NG_006672.1:g.7849T>A , LRG_429:g.7849T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*251T>A ENSP00000355644.4:n.*251T>A
ENST00000684723.1:c.*251T>A ENSP00000508084.1:n.*251T>A
ENST00000366684.7:c.*251T>A MANE Select ENSP00000355645.3:n.*251T>A
NM_001100.3:c.*251T>A , LRG_429t1:c.*251T>A NP_001091.1:n.*251T>A
NM_001100.4:c.*251T>A MANE Select NP_001091.1:n.*251T>A
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