Canonical Allele Identifier: CA732579040
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1200767464
MyVariant Identifiers: chr1:g.229566990A>T (hg19) chr1:g.229431243A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431243A>T , CM000663.2:g.229431243A>T GRCh38
NC_000001.10:g.229566990A>T , CM000663.1:g.229566990A>T GRCh37
NC_000001.9:g.227633613A>T NCBI36
NG_006672.1:g.7854T>A , LRG_429:g.7854T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684723.1:c.*256T>A ENSP00000508084.1:n.*256T>A
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