Canonical Allele Identifier: CA345146669
Gene: ACTA1 HGNC NCBI

Linked Data

gnomAD v4: 1-229432048-T-C
MyVariant Identifiers: chr1:g.229567795T>C (hg19) chr1:g.229432048T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432048T>C , CM000663.2:g.229432048T>C GRCh38
NC_000001.10:g.229567795T>C , CM000663.1:g.229567795T>C GRCh37
NC_000001.9:g.227634418T>C NCBI36
NG_006672.1:g.7049A>G , LRG_429:g.7049A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.754A>G ENSP00000355644.4:p.Ile252Val
ENST00000684723.1:c.619A>G ENSP00000508084.1:p.Ile207Val
ENST00000366683.3:c.480-186A>G ENSP00000355644.3:n.480-186A>G
ENST00000366684.7:c.754A>G MANE Select ENSP00000355645.3:p.Ile252Val
NM_001100.3:c.754A>G , LRG_429t1:c.754A>G NP_001091.1:p.Ile252Val
NM_001100.4:c.754A>G MANE Select NP_001091.1:p.Ile252Val
Search 100 bp 5'
Search 100 bp 3'