Canonical Allele Identifier: CA2453332074
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922542635
gnomAD v4: X-116173586-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173586T>C , CM000685.2:g.116173586T>C GRCh38
NC_000023.10:g.115304839T>C , CM000685.1:g.115304839T>C GRCh37
NC_000023.9:g.115218867T>C NCBI36
NG_016326.1:g.7882T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*214T>C MANE Select ENSP00000360973.4:n.*214T>C
ENST00000371906.4:c.*214T>C ENSP00000360973.4:n.*214T>C
NM_000686.4:c.*214T>C NP_000677.2:n.*214T>C
XM_011537533.1:c.*214T>C XP_011535835.1:n.*214T>C
NM_000686.5:c.*214T>C MANE Select NP_000677.2:n.*214T>C
NM_001385624.1:c.*214T>C NP_001372553.1:n.*214T>C
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