Canonical Allele Identifier: CA10976126
Gene: AGT HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs2478545

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230708375G>A , CM000663.2:g.230708375G>A GRCh38
NC_000001.10:g.230844121G>A , CM000663.1:g.230844121G>A GRCh37
NC_000001.9:g.228910744G>A NCBI36
NG_008836.1:g.11216C>T
NG_008836.2:g.11216C>T

Transcript Alleles

HGVS Amino-acid change
NM_000029.3:c.856+1620C>T VV NP_000020.1:p.=
NM_000029.4:c.856+1620C>T VV MANE Preferred NP_000020.1:p.=
ENST00000366667.4:c.856+1620C>T ENSP00000355627.4:p.=