Canonical Allele Identifier: CA644065571

Gene: AGTR2

Linked Data

• dbSNP Id: rs1333073750
• gnomAD v2: X-115303532-A-G
• gnomAD v3: X-116172279-A-G
• gnomAD v4: X-116172279-A-G
• MyVariant Identifiers: chrX:g.115303532A>G (hg19) ; chrX:g.116172279A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172279A>G , CM000685.2:g.116172279A>G	GRCh38
NC_000023.10:g.115303532A>G , CM000685.1:g.115303532A>G	GRCh37
NC_000023.9:g.115217560A>G	NCBI36
NG_016326.1:g.6575A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.-2A>G MANE Select	ENSP00000360973.4:n.-2A>G
ENST00000680409.1:n.467A>G
ENST00000681852.1:c.-2A>G	ENSP00000505750.1:n.-2A>G
ENST00000371906.4:c.-2A>G	ENSP00000360973.4:n.-2A>G
NM_000686.4:c.-2A>G	NP_000677.2:n.-2A>G
XM_011537533.1:c.-2A>G	XP_011535835.1:n.-2A>G
NM_000686.5:c.-2A>G MANE Select	NP_000677.2:n.-2A>G
NM_001385624.1:c.-2A>G	NP_001372553.1:n.-2A>G