Canonical Allele Identifier: CA732578999
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1453768341
MyVariant Identifiers: chr1:g.229566853G>A (hg19) chr1:g.229431106G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431106G>A , CM000663.2:g.229431106G>A GRCh38
NC_000001.10:g.229566853G>A , CM000663.1:g.229566853G>A GRCh37
NC_000001.9:g.227633476G>A NCBI36
NG_006672.1:g.7991C>T , LRG_429:g.7991C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684723.1:c.*393C>T ENSP00000508084.1:n.*393C>T
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