Canonical Allele Identifier: CA414337554
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115303615A>G (hg19) chrX:g.116172362A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172362A>G , CM000685.2:g.116172362A>G GRCh38
NC_000023.10:g.115303615A>G , CM000685.1:g.115303615A>G GRCh37
NC_000023.9:g.115217643A>G NCBI36
NG_016326.1:g.6658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.82A>G MANE Select ENSP00000360973.4:p.Asn28Asp
ENST00000680409.1:n.550A>G
ENST00000681852.1:c.82A>G ENSP00000505750.1:p.Asn28Asp
ENST00000371906.4:c.82A>G ENSP00000360973.4:p.Asn28Asp
NM_000686.4:c.82A>G NP_000677.2:p.Asn28Asp
XM_011537533.1:c.82A>G XP_011535835.1:p.Asn28Asp
NM_000686.5:c.82A>G MANE Select NP_000677.2:p.Asn28Asp
NM_001385624.1:c.82A>G NP_001372553.1:p.Asn28Asp
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