Canonical Allele Identifier: CA334723670
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs368409134
gnomAD v2: X-115303376-T-G
gnomAD v3: X-116172123-T-G
gnomAD v4: X-116172123-T-G
MyVariant Identifiers: chrX:g.115303376T>G (hg19) chrX:g.116172123T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172123T>G , CM000685.2:g.116172123T>G GRCh38
NC_000023.10:g.115303376T>G , CM000685.1:g.115303376T>G GRCh37
NC_000023.9:g.115217404T>G NCBI36
NG_016326.1:g.6419T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-123T>G MANE Select ENSP00000360973.4:n.-35-123T>G
ENST00000680409.1:n.311T>G
ENST00000681852.1:c.-35-123T>G ENSP00000505750.1:n.-35-123T>G
ENST00000371906.4:c.-35-123T>G ENSP00000360973.4:n.-35-123T>G
NM_000686.4:c.-35-123T>G NP_000677.2:n.-35-123T>G
XM_011537533.1:c.-35-123T>G XP_011535835.1:n.-35-123T>G
NM_000686.5:c.-35-123T>G MANE Select NP_000677.2:n.-35-123T>G
NM_001385624.1:c.-35-123T>G NP_001372553.1:n.-35-123T>G
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