Canonical Allele Identifier: CA423755036
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs2102735935
MyVariant Identifiers: chr1:g.229568108G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229432361G>A , CM000663.2:g.229432361G>A GRCh38
NC_000001.10:g.229568108G>A , CM000663.1:g.229568108G>A GRCh37
NC_000001.9:g.227634731G>A NCBI36
NG_006672.1:g.6736C>T , LRG_429:g.6736C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366683.4:c.525C>T ENSP00000355644.4:p.His175=
ENST00000684723.1:c.390C>T ENSP00000508084.1:p.His130=
ENST00000366683.3:c.479+46C>T ENSP00000355644.3:n.479+46C>T
ENST00000366684.7:c.525C>T MANE Select ENSP00000355645.3:p.His175=
NM_001100.3:c.525C>T , LRG_429t1:c.525C>T NP_001091.1:p.His175=
NM_001100.4:c.525C>T MANE Select NP_001091.1:p.His175=