Canonical Allele Identifier: CA2694510835
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116172200-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172200C>A , CM000685.2:g.116172200C>A GRCh38
NC_000023.10:g.115303453C>A , CM000685.1:g.115303453C>A GRCh37
NC_000023.9:g.115217481C>A NCBI36
NG_016326.1:g.6496C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-46C>A MANE Select ENSP00000360973.4:n.-35-46C>A
ENST00000680409.1:n.388C>A
ENST00000681852.1:c.-35-46C>A ENSP00000505750.1:n.-35-46C>A
ENST00000371906.4:c.-35-46C>A ENSP00000360973.4:n.-35-46C>A
NM_000686.4:c.-35-46C>A NP_000677.2:n.-35-46C>A
XM_011537533.1:c.-35-46C>A XP_011535835.1:n.-35-46C>A
NM_000686.5:c.-35-46C>A MANE Select NP_000677.2:n.-35-46C>A
NM_001385624.1:c.-35-46C>A NP_001372553.1:n.-35-46C>A
Search 100 bp 5'
Search 100 bp 3'