Canonical Allele Identifier: CA518287046
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173264-G-A
MyVariant Identifiers: chrX:g.115304517G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173264G>A , CM000685.2:g.116173264G>A GRCh38
NC_000023.10:g.115304517G>A , CM000685.1:g.115304517G>A GRCh37
NC_000023.9:g.115218545G>A NCBI36
NG_016326.1:g.7560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.984G>A MANE Select ENSP00000360973.4:p.Lys328=
ENST00000680409.1:n.1452G>A
ENST00000681852.1:c.984G>A ENSP00000505750.1:p.Lys328=
ENST00000371906.4:c.984G>A ENSP00000360973.4:p.Lys328=
NM_000686.4:c.984G>A NP_000677.2:p.Lys328=
XM_011537533.1:c.984G>A XP_011535835.1:p.Lys328=
NM_000686.5:c.984G>A MANE Select NP_000677.2:p.Lys328=
NM_001385624.1:c.984G>A NP_001372553.1:p.Lys328=
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