Canonical Allele Identifier: CA518287060
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1922528965
MyVariant Identifiers: chrX:g.115304532T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173279T>C , CM000685.2:g.116173279T>C GRCh38
NC_000023.10:g.115304532T>C , CM000685.1:g.115304532T>C GRCh37
NC_000023.9:g.115218560T>C NCBI36
NG_016326.1:g.7575T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.999T>C MANE Select ENSP00000360973.4:p.Phe333=
ENST00000680409.1:n.1467T>C
ENST00000681852.1:c.999T>C ENSP00000505750.1:p.Phe333=
ENST00000371906.4:c.999T>C ENSP00000360973.4:p.Phe333=
NM_000686.4:c.999T>C NP_000677.2:p.Phe333=
XM_011537533.1:c.999T>C XP_011535835.1:p.Phe333=
NM_000686.5:c.999T>C MANE Select NP_000677.2:p.Phe333=
NM_001385624.1:c.999T>C NP_001372553.1:p.Phe333=
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