Canonical Allele Identifier: CA345147495
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1267307077

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432179C>T , CM000663.2:g.229432179C>T GRCh38
NC_000001.10:g.229567926C>T , CM000663.1:g.229567926C>T GRCh37
NC_000001.9:g.227634549C>T NCBI36
NG_006672.1:g.6918G>A , LRG_429:g.6918G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.623G>A ENSP00000355644.4:p.Arg208His
ENST00000684723.1:c.488G>A ENSP00000508084.1:p.Arg163His
ENST00000366683.3:c.479+228G>A ENSP00000355644.3:n.479+228G>A
ENST00000366684.7:c.623G>A MANE Select ENSP00000355645.3:p.Arg208His
NM_001100.3:c.623G>A , LRG_429t1:c.623G>A NP_001091.1:p.Arg208His
NM_001100.4:c.623G>A MANE Select NP_001091.1:p.Arg208His