Canonical Allele Identifier: CA732582778
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs750053890
gnomAD v3: 1-229432961-C-T
gnomAD v4: 1-229432961-C-T
MyVariant Identifiers: chr1:g.229568708C>T (hg19) chr1:g.229432961C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432961C>T , CM000663.2:g.229432961C>T GRCh38
NC_000001.10:g.229568708C>T , CM000663.1:g.229568708C>T GRCh37
NC_000001.9:g.227635331C>T NCBI36
NG_006672.1:g.6136G>A , LRG_429:g.6136G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.129+26G>A ENSP00000355644.4:n.129+26G>A
ENST00000684723.1:c.-6-81G>A ENSP00000508084.1:n.-6-81G>A
ENST00000366683.3:c.129+26G>A ENSP00000355644.3:n.129+26G>A
ENST00000366684.7:c.129+26G>A MANE Select ENSP00000355645.3:n.129+26G>A
NM_001100.3:c.129+26G>A , LRG_429t1:c.129+26G>A NP_001091.1:n.129+26G>A
NM_001100.4:c.129+26G>A MANE Select NP_001091.1:n.129+26G>A
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