Canonical Allele Identifier: CA1226669974
Gene: AGT HGNC NCBI

Linked Data

dbSNP Id: rs1663737361
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230716367C>T , CM000663.2:g.230716367C>T GRCh38
NC_000001.10:g.230852113C>T , CM000663.1:g.230852113C>T GRCh37
NC_000001.9:g.228918736C>T NCBI36
NG_008836.1:g.3224G>A
NG_008836.2:g.3224G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000681269.1:c.-30-5514G>A ENSP00000505985.1:n.-30-5514G>A
NM_001382817.3:c.-30-5514G>A NP_001369746.2:n.-30-5514G>A
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