Canonical Allele Identifier: CA414337541

Gene: AGTR2

Linked Data

• ClinVar Variation Id: 2309091
• ClinVar RCV Id: RCV002870291
• MyVariant Identifiers: chrX:g.115303609T>C (hg19) ; chrX:g.116172356T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172356T>C , CM000685.2:g.116172356T>C	GRCh38
NC_000023.10:g.115303609T>C , CM000685.1:g.115303609T>C	GRCh37
NC_000023.9:g.115217637T>C	NCBI36
NG_016326.1:g.6652T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371906.5:c.76T>C MANE Select	ENSP00000360973.4:p.Ser26Pro
ENST00000680409.1:n.544T>C
ENST00000681852.1:c.76T>C	ENSP00000505750.1:p.Ser26Pro
ENST00000371906.4:c.76T>C	ENSP00000360973.4:p.Ser26Pro
NM_000686.4:c.76T>C	NP_000677.2:p.Ser26Pro
XM_011537533.1:c.76T>C	XP_011535835.1:p.Ser26Pro
NM_000686.5:c.76T>C MANE Select	NP_000677.2:p.Ser26Pro
NM_001385624.1:c.76T>C	NP_001372553.1:p.Ser26Pro