Canonical Allele Identifier: CA2694510890
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173413-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173413T>A , CM000685.2:g.116173413T>A GRCh38
NC_000023.10:g.115304666T>A , CM000685.1:g.115304666T>A GRCh37
NC_000023.9:g.115218694T>A NCBI36
NG_016326.1:g.7709T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*41T>A MANE Select ENSP00000360973.4:n.*41T>A
ENST00000680409.1:n.1601T>A
ENST00000371906.4:c.*41T>A ENSP00000360973.4:n.*41T>A
NM_000686.4:c.*41T>A NP_000677.2:n.*41T>A
XM_011537533.1:c.*41T>A XP_011535835.1:n.*41T>A
NM_000686.5:c.*41T>A MANE Select NP_000677.2:n.*41T>A
NM_001385624.1:c.*41T>A NP_001372553.1:n.*41T>A
Search 100 bp 5'
Search 100 bp 3'