Canonical Allele Identifier: CA644065623

Gene: AGTR2

Linked Data

• dbSNP Id: rs1556673697
• gnomAD v2: X-115303763-A-AAAAGTGAGT
• MyVariant Identifiers: chrX:g.115303763_115303764insAAAGTGAGT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.116172510_116172511insAAAGTGAGT , CM000685.2:g.116172510_116172511insAAAGTGAGT	GRCh38
NC_000023.10:g.115303763_115303764insAAAGTGAGT , CM000685.1:g.115303763_115303764insAAAGTGAGT	GRCh37
NC_000023.9:g.115217791_115217792insAAAGTGAGT	NCBI36
NG_016326.1:g.6806_6807insAAAGTGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371906.5:c.230_231insAAAGTGAGT MANE Select	ENSP00000360973.4:p.Lys78LysfsTer2
ENST00000680409.1:n.698_699insAAAGTGAGT
ENST00000681852.1:c.230_231insAAAGTGAGT	ENSP00000505750.1:p.Lys78LysfsTer2
ENST00000371906.4:c.230_231insAAAGTGAGT	ENSP00000360973.4:p.Lys78LysfsTer2
NM_000686.4:c.230_231insAAAGTGAGT	NP_000677.2:p.Lys78LysfsTer2
XM_011537533.1:c.230_231insAAAGTGAGT	XP_011535835.1:p.Lys78LysfsTer2
NM_000686.5:c.230_231insAAAGTGAGT MANE Select	NP_000677.2:p.Lys78LysfsTer2
NM_001385624.1:c.230_231insAAAGTGAGT	NP_001372553.1:p.Lys78LysfsTer2