Canonical Allele Identifier: CA414337859
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1556673692
gnomAD v4: X-116172500-G-C
MyVariant Identifiers: chrX:g.115303753G>C (hg19) chrX:g.116172500G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172500G>C , CM000685.2:g.116172500G>C GRCh38
NC_000023.10:g.115303753G>C , CM000685.1:g.115303753G>C GRCh37
NC_000023.9:g.115217781G>C NCBI36
NG_016326.1:g.6796G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.220G>C MANE Select ENSP00000360973.4:p.Gly74Arg
ENST00000680409.1:n.688G>C
ENST00000681852.1:c.220G>C ENSP00000505750.1:p.Gly74Arg
ENST00000371906.4:c.220G>C ENSP00000360973.4:p.Gly74Arg
NM_000686.4:c.220G>C NP_000677.2:p.Gly74Arg
XM_011537533.1:c.220G>C XP_011535835.1:p.Gly74Arg
NM_000686.5:c.220G>C MANE Select NP_000677.2:p.Gly74Arg
NM_001385624.1:c.220G>C NP_001372553.1:p.Gly74Arg
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