Canonical Allele Identifier: CA870448251
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1255668191
gnomAD v3: X-116172208-T-C
gnomAD v4: X-116172208-T-C
MyVariant Identifiers: chrX:g.116172208T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172208T>C , CM000685.2:g.116172208T>C GRCh38
NC_000023.10:g.115303461T>C , CM000685.1:g.115303461T>C GRCh37
NC_000023.9:g.115217489T>C NCBI36
NG_016326.1:g.6504T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.-35-38T>C MANE Select ENSP00000360973.4:n.-35-38T>C
ENST00000680409.1:n.396T>C
ENST00000681852.1:c.-35-38T>C ENSP00000505750.1:n.-35-38T>C
ENST00000371906.4:c.-35-38T>C ENSP00000360973.4:n.-35-38T>C
NM_000686.4:c.-35-38T>C NP_000677.2:n.-35-38T>C
XM_011537533.1:c.-35-38T>C XP_011535835.1:n.-35-38T>C
NM_000686.5:c.-35-38T>C MANE Select NP_000677.2:n.-35-38T>C
NM_001385624.1:c.-35-38T>C NP_001372553.1:n.-35-38T>C
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