Canonical Allele Identifier: CA1136568795
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922470496
gnomAD v3: X-116172198-T-A
gnomAD v4: X-116172198-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172198T>A , CM000685.2:g.116172198T>A GRCh38
NC_000023.10:g.115303451T>A , CM000685.1:g.115303451T>A GRCh37
NC_000023.9:g.115217479T>A NCBI36
NG_016326.1:g.6494T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-48T>A MANE Select ENSP00000360973.4:n.-35-48T>A
ENST00000680409.1:n.386T>A
ENST00000681852.1:c.-35-48T>A ENSP00000505750.1:n.-35-48T>A
ENST00000371906.4:c.-35-48T>A ENSP00000360973.4:n.-35-48T>A
NM_000686.4:c.-35-48T>A NP_000677.2:n.-35-48T>A
XM_011537533.1:c.-35-48T>A XP_011535835.1:n.-35-48T>A
NM_000686.5:c.-35-48T>A MANE Select NP_000677.2:n.-35-48T>A
NM_001385624.1:c.-35-48T>A NP_001372553.1:n.-35-48T>A
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