Canonical Allele Identifier: CA1226125576
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1558081555
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431941G>T , CM000663.2:g.229431941G>T GRCh38
NC_000001.10:g.229567688G>T , CM000663.1:g.229567688G>T GRCh37
NC_000001.9:g.227634311G>T NCBI36
NG_006672.1:g.7156C>A , LRG_429:g.7156C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.809-39C>A ENSP00000355644.4:n.809-39C>A
ENST00000684723.1:c.674-39C>A ENSP00000508084.1:n.674-39C>A
ENST00000366683.3:c.480-79C>A ENSP00000355644.3:n.480-79C>A
ENST00000366684.7:c.809-39C>A MANE Select ENSP00000355645.3:n.809-39C>A
NM_001100.3:c.809-39C>A , LRG_429t1:c.809-39C>A NP_001091.1:n.809-39C>A
NM_001100.4:c.809-39C>A MANE Select NP_001091.1:n.809-39C>A
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