Canonical Allele Identifier: CA2453332008
Gene: AGTR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173382C= , CM000685.2:g.116173382C= GRCh38
NC_000023.10:g.115304635C= , CM000685.1:g.115304635C= GRCh37
NC_000023.9:g.115218663C= NCBI36
NG_016326.1:g.7678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*10C= MANE Select ENSP00000360973.4:n.*10C=
ENST00000680409.1:n.1570C=
ENST00000371906.4:c.*10C= ENSP00000360973.4:n.*10C=
NM_000686.4:c.*10C= NP_000677.2:n.*10C=
XM_011537533.1:c.*10C= XP_011535835.1:n.*10C=
NM_000686.5:c.*10C= MANE Select NP_000677.2:n.*10C=
NM_001385624.1:c.*10C= NP_001372553.1:n.*10C=
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