Canonical Allele Identifier: CA518449615

Gene: AGTR2

Linked Data

• gnomAD v4: X-116172613-C-T
• COSMIC: COSM5599038
• MyVariant Identifiers: chrX:g.115303866C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172613C>T , CM000685.2:g.116172613C>T	GRCh38
NC_000023.10:g.115303866C>T , CM000685.1:g.115303866C>T	GRCh37
NC_000023.9:g.115217894C>T	NCBI36
NG_016326.1:g.6909C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.333C>T MANE Select	ENSP00000360973.4:p.Leu111=
ENST00000680409.1:n.801C>T
ENST00000681852.1:c.333C>T	ENSP00000505750.1:p.Leu111=
ENST00000371906.4:c.333C>T	ENSP00000360973.4:p.Leu111=
NM_000686.4:c.333C>T	NP_000677.2:p.Leu111=
XM_011537533.1:c.333C>T	XP_011535835.1:p.Leu111=
NM_000686.5:c.333C>T MANE Select	NP_000677.2:p.Leu111=
NM_001385624.1:c.333C>T	NP_001372553.1:p.Leu111=