Canonical Allele Identifier: CA38814459
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1027851092
gnomAD v4: 1-229431178-G-C
MyVariant Identifiers: chr1:g.229566925G>C (hg19) chr1:g.229431178G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431178G>C , CM000663.2:g.229431178G>C GRCh38
NC_000001.10:g.229566925G>C , CM000663.1:g.229566925G>C GRCh37
NC_000001.9:g.227633548G>C NCBI36
NG_006672.1:g.7919C>G , LRG_429:g.7919C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684723.1:c.*321C>G ENSP00000508084.1:n.*321C>G
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