Canonical Allele Identifier: CA2453332068
Gene: AGTR2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173571G= , CM000685.2:g.116173571G= GRCh38
NC_000023.10:g.115304824G= , CM000685.1:g.115304824G= GRCh37
NC_000023.9:g.115218852G= NCBI36
NG_016326.1:g.7867G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*199G= MANE Select ENSP00000360973.4:n.*199G=
ENST00000371906.4:c.*199G= ENSP00000360973.4:n.*199G=
NM_000686.4:c.*199G= NP_000677.2:n.*199G=
XM_011537533.1:c.*199G= XP_011535835.1:n.*199G=
NM_000686.5:c.*199G= MANE Select NP_000677.2:n.*199G=
NM_001385624.1:c.*199G= NP_001372553.1:n.*199G=
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