Canonical Allele Identifier: CA518449097
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115303548C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172295C>A , CM000685.2:g.116172295C>A GRCh38
NC_000023.10:g.115303548C>A , CM000685.1:g.115303548C>A GRCh37
NC_000023.9:g.115217576C>A NCBI36
NG_016326.1:g.6591C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.15C>A MANE Select ENSP00000360973.4:p.Ser5=
ENST00000680409.1:n.483C>A
ENST00000681852.1:c.15C>A ENSP00000505750.1:p.Ser5=
ENST00000371906.4:c.15C>A ENSP00000360973.4:p.Ser5=
NM_000686.4:c.15C>A NP_000677.2:p.Ser5=
XM_011537533.1:c.15C>A XP_011535835.1:p.Ser5=
NM_000686.5:c.15C>A MANE Select NP_000677.2:p.Ser5=
NM_001385624.1:c.15C>A NP_001372553.1:p.Ser5=
Search 100 bp 5'
Search 100 bp 3'