Canonical Allele Identifier: CA2694511019

Gene: AGTR2

Linked Data

• gnomAD v4: X-116173618-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116173618C>T , CM000685.2:g.116173618C>T	GRCh38
NC_000023.10:g.115304871C>T , CM000685.1:g.115304871C>T	GRCh37
NC_000023.9:g.115218899C>T	NCBI36
NG_016326.1:g.7914C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.*246C>T MANE Select	ENSP00000360973.4:n.*246C>T
ENST00000371906.4:c.*246C>T	ENSP00000360973.4:n.*246C>T
NM_000686.4:c.*246C>T	NP_000677.2:n.*246C>T
XM_011537533.1:c.*246C>T	XP_011535835.1:n.*246C>T
NM_000686.5:c.*246C>T MANE Select	NP_000677.2:n.*246C>T
NM_001385624.1:c.*246C>T	NP_001372553.1:n.*246C>T