Canonical Allele Identifier: CA2698170032
Gene: ACTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1200046209

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431101G>C , CM000663.2:g.229431101G>C GRCh38
NC_000001.10:g.229566848G>C , CM000663.1:g.229566848G>C GRCh37
NC_000001.9:g.227633471G>C NCBI36
NG_006672.1:g.7996C>G , LRG_429:g.7996C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684723.1:c.*398C>G ENSP00000508084.1:n.*398C>G