Canonical Allele Identifier: CA2600295487
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs2147302742
gnomAD v3: X-116173582-G-A
gnomAD v4: X-116173582-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173582G>A , CM000685.2:g.116173582G>A GRCh38
NC_000023.10:g.115304835G>A , CM000685.1:g.115304835G>A GRCh37
NC_000023.9:g.115218863G>A NCBI36
NG_016326.1:g.7878G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*210G>A MANE Select ENSP00000360973.4:n.*210G>A
ENST00000371906.4:c.*210G>A ENSP00000360973.4:n.*210G>A
NM_000686.4:c.*210G>A NP_000677.2:n.*210G>A
XM_011537533.1:c.*210G>A XP_011535835.1:n.*210G>A
NM_000686.5:c.*210G>A MANE Select NP_000677.2:n.*210G>A
NM_001385624.1:c.*210G>A NP_001372553.1:n.*210G>A
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