Canonical Allele Identifier: CA414337549
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115303613G>A (hg19) chrX:g.116172360G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172360G>A , CM000685.2:g.116172360G>A GRCh38
NC_000023.10:g.115303613G>A , CM000685.1:g.115303613G>A GRCh37
NC_000023.9:g.115217641G>A NCBI36
NG_016326.1:g.6656G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.80G>A MANE Select ENSP00000360973.4:p.Gly27Asp
ENST00000680409.1:n.548G>A
ENST00000681852.1:c.80G>A ENSP00000505750.1:p.Gly27Asp
ENST00000371906.4:c.80G>A ENSP00000360973.4:p.Gly27Asp
NM_000686.4:c.80G>A NP_000677.2:p.Gly27Asp
XM_011537533.1:c.80G>A XP_011535835.1:p.Gly27Asp
NM_000686.5:c.80G>A MANE Select NP_000677.2:p.Gly27Asp
NM_001385624.1:c.80G>A NP_001372553.1:p.Gly27Asp
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