Canonical Allele Identifier: CA334723702

Gene: AGTR2

Linked Data

• dbSNP Id: rs181669267
• gnomAD v2: X-115304735-A-C
• gnomAD v3: X-116173482-A-C
• gnomAD v4: X-116173482-A-C
• MyVariant Identifiers: chrX:g.115304735A>C (hg19) ; chrX:g.116173482A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116173482A>C , CM000685.2:g.116173482A>C	GRCh38
NC_000023.10:g.115304735A>C , CM000685.1:g.115304735A>C	GRCh37
NC_000023.9:g.115218763A>C	NCBI36
NG_016326.1:g.7778A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.*110A>C MANE Select	ENSP00000360973.4:n.*110A>C
ENST00000371906.4:c.*110A>C	ENSP00000360973.4:n.*110A>C
NM_000686.4:c.*110A>C	NP_000677.2:n.*110A>C
XM_011537533.1:c.*110A>C	XP_011535835.1:n.*110A>C
NM_000686.5:c.*110A>C MANE Select	NP_000677.2:n.*110A>C
NM_001385624.1:c.*110A>C	NP_001372553.1:n.*110A>C