Canonical Allele Identifier: CA1442827
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs756483510
ExAC: 1:229567962 C / T
gnomAD v2: 1-229567962-C-T
gnomAD v4: 1-229432215-C-T
MyVariant Identifiers: chr1:g.229567962C>T (hg19) chr1:g.229432215C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432215C>T , CM000663.2:g.229432215C>T GRCh38
NC_000001.10:g.229567962C>T , CM000663.1:g.229567962C>T GRCh37
NC_000001.9:g.227634585C>T NCBI36
NG_006672.1:g.6882G>A , LRG_429:g.6882G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.617-30G>A ENSP00000355644.4:n.617-30G>A
ENST00000684723.1:c.482-30G>A ENSP00000508084.1:n.482-30G>A
ENST00000366683.3:c.479+192G>A ENSP00000355644.3:n.479+192G>A
ENST00000366684.7:c.617-30G>A MANE Select ENSP00000355645.3:n.617-30G>A
NM_001100.3:c.617-30G>A , LRG_429t1:c.617-30G>A NP_001091.1:n.617-30G>A
NM_001100.4:c.617-30G>A MANE Select NP_001091.1:n.617-30G>A
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