Canonical Allele Identifier: CA2453331632
Gene: AGTR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172224G= , CM000685.2:g.116172224G= GRCh38
NC_000023.10:g.115303477G= , CM000685.1:g.115303477G= GRCh37
NC_000023.9:g.115217505G= NCBI36
NG_016326.1:g.6520G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-22G= MANE Select ENSP00000360973.4:n.-35-22G=
ENST00000680409.1:n.412G=
ENST00000681852.1:c.-35-22G= ENSP00000505750.1:n.-35-22G=
ENST00000371906.4:c.-35-22G= ENSP00000360973.4:n.-35-22G=
NM_000686.4:c.-35-22G= NP_000677.2:n.-35-22G=
XM_011537533.1:c.-35-22G= XP_011535835.1:n.-35-22G=
NM_000686.5:c.-35-22G= MANE Select NP_000677.2:n.-35-22G=
NM_001385624.1:c.-35-22G= NP_001372553.1:n.-35-22G=
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