Canonical Allele Identifier: CA1136568731
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922464348
gnomAD v3: X-116172018-C-T
gnomAD v4: X-116172018-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172018C>T , CM000685.2:g.116172018C>T GRCh38
NC_000023.10:g.115303271C>T , CM000685.1:g.115303271C>T GRCh37
NC_000023.9:g.115217299C>T NCBI36
NG_016326.1:g.6314C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-228C>T MANE Select ENSP00000360973.4:n.-35-228C>T
ENST00000680409.1:n.206C>T
ENST00000681852.1:c.-35-228C>T ENSP00000505750.1:n.-35-228C>T
ENST00000371906.4:c.-35-228C>T ENSP00000360973.4:n.-35-228C>T
NM_000686.4:c.-35-228C>T NP_000677.2:n.-35-228C>T
XM_011537533.1:c.-35-228C>T XP_011535835.1:n.-35-228C>T
NM_000686.5:c.-35-228C>T MANE Select NP_000677.2:n.-35-228C>T
NM_001385624.1:c.-35-228C>T NP_001372553.1:n.-35-228C>T
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