Canonical Allele Identifier: CA2453332067
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922540954
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173570T>G , CM000685.2:g.116173570T>G GRCh38
NC_000023.10:g.115304823T>G , CM000685.1:g.115304823T>G GRCh37
NC_000023.9:g.115218851T>G NCBI36
NG_016326.1:g.7866T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*198T>G MANE Select ENSP00000360973.4:n.*198T>G
ENST00000371906.4:c.*198T>G ENSP00000360973.4:n.*198T>G
NM_000686.4:c.*198T>G NP_000677.2:n.*198T>G
XM_011537533.1:c.*198T>G XP_011535835.1:n.*198T>G
NM_000686.5:c.*198T>G MANE Select NP_000677.2:n.*198T>G
NM_001385624.1:c.*198T>G NP_001372553.1:n.*198T>G
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