Canonical Allele Identifier: CA38815737
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs538086483
gnomAD v4: 1-229432154-C-T
MyVariant Identifiers: chr1:g.229567901C>T (hg19) chr1:g.229432154C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432154C>T , CM000663.2:g.229432154C>T GRCh38
NC_000001.10:g.229567901C>T , CM000663.1:g.229567901C>T GRCh37
NC_000001.9:g.227634524C>T NCBI36
NG_006672.1:g.6943G>A , LRG_429:g.6943G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.648G>A ENSP00000355644.4:p.Glu216=
ENST00000684723.1:c.513G>A ENSP00000508084.1:p.Glu171=
ENST00000366683.3:c.479+253G>A ENSP00000355644.3:n.479+253G>A
ENST00000366684.7:c.648G>A MANE Select ENSP00000355645.3:p.Glu216=
NM_001100.3:c.648G>A , LRG_429t1:c.648G>A NP_001091.1:p.Glu216=
NM_001100.4:c.648G>A MANE Select NP_001091.1:p.Glu216=
Search 100 bp 5'
Search 100 bp 3'