Canonical Allele Identifier: CA10497222

Gene: AGTR2

Linked Data

• dbSNP Id: rs371106264
• ExAC: X:115303551 C / T
• gnomAD v2: X-115303551-C-T
• gnomAD v3: X-116172298-C-T
• gnomAD v4: X-116172298-C-T
• MyVariant Identifiers: chrX:g.115303551C>T (hg19) ; chrX:g.116172298C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172298C>T , CM000685.2:g.116172298C>T	GRCh38
NC_000023.10:g.115303551C>T , CM000685.1:g.115303551C>T	GRCh37
NC_000023.9:g.115217579C>T	NCBI36
NG_016326.1:g.6594C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.18C>T MANE Select	ENSP00000360973.4:p.Thr6=
ENST00000680409.1:n.486C>T
ENST00000681852.1:c.18C>T	ENSP00000505750.1:p.Thr6=
ENST00000371906.4:c.18C>T	ENSP00000360973.4:p.Thr6=
NM_000686.4:c.18C>T	NP_000677.2:p.Thr6=
XM_011537533.1:c.18C>T	XP_011535835.1:p.Thr6=
NM_000686.5:c.18C>T MANE Select	NP_000677.2:p.Thr6=
NM_001385624.1:c.18C>T	NP_001372553.1:p.Thr6=