Canonical Allele Identifier: CA414337387
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116172288-G-A
MyVariant Identifiers: chrX:g.115303541G>A (hg19) chrX:g.116172288G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172288G>A , CM000685.2:g.116172288G>A GRCh38
NC_000023.10:g.115303541G>A , CM000685.1:g.115303541G>A GRCh37
NC_000023.9:g.115217569G>A NCBI36
NG_016326.1:g.6584G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.8G>A MANE Select ENSP00000360973.4:p.Gly3Asp
ENST00000680409.1:n.476G>A
ENST00000681852.1:c.8G>A ENSP00000505750.1:p.Gly3Asp
ENST00000371906.4:c.8G>A ENSP00000360973.4:p.Gly3Asp
NM_000686.4:c.8G>A NP_000677.2:p.Gly3Asp
XM_011537533.1:c.8G>A XP_011535835.1:p.Gly3Asp
NM_000686.5:c.8G>A MANE Select NP_000677.2:p.Gly3Asp
NM_001385624.1:c.8G>A NP_001372553.1:p.Gly3Asp
Search 100 bp 5'
Search 100 bp 3'