Canonical Allele Identifier: CA38877098
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs939622642

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716331T>C , CM000663.2:g.230716331T>C GRCh38
NC_000001.10:g.230852077T>C , CM000663.1:g.230852077T>C GRCh37
NC_000001.9:g.228918700T>C NCBI36
NG_008836.1:g.3260A>G
NG_008836.2:g.3260A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000681269.1:c.-30-5478A>G ENSP00000505985.1:n.-30-5478A>G
NM_001382817.3:c.-30-5478A>G NP_001369746.2:n.-30-5478A>G