Canonical Allele Identifier: CA518287091
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115304559G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173306G>C , CM000685.2:g.116173306G>C GRCh38
NC_000023.10:g.115304559G>C , CM000685.1:g.115304559G>C GRCh37
NC_000023.9:g.115218587G>C NCBI36
NG_016326.1:g.7602G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.1026G>C MANE Select ENSP00000360973.4:p.Gly342=
ENST00000680409.1:n.1494G>C
ENST00000681852.1:c.1026G>C ENSP00000505750.1:p.Gly342=
ENST00000371906.4:c.1026G>C ENSP00000360973.4:p.Gly342=
NM_000686.4:c.1026G>C NP_000677.2:p.Gly342=
XM_011537533.1:c.1026G>C XP_011535835.1:p.Gly342=
NM_000686.5:c.1026G>C MANE Select NP_000677.2:p.Gly342=
NM_001385624.1:c.1026G>C NP_001372553.1:p.Gly342=
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