Canonical Allele Identifier: CA2453331615
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1556673647

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172190C>G , CM000685.2:g.116172190C>G GRCh38
NC_000023.10:g.115303443C>G , CM000685.1:g.115303443C>G GRCh37
NC_000023.9:g.115217471C>G NCBI36
NG_016326.1:g.6486C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-56C>G MANE Select ENSP00000360973.4:n.-35-56C>G
ENST00000680409.1:n.378C>G
ENST00000681852.1:c.-35-56C>G ENSP00000505750.1:n.-35-56C>G
ENST00000371906.4:c.-35-56C>G ENSP00000360973.4:n.-35-56C>G
NM_000686.4:c.-35-56C>G NP_000677.2:n.-35-56C>G
XM_011537533.1:c.-35-56C>G XP_011535835.1:n.-35-56C>G
NM_000686.5:c.-35-56C>G MANE Select NP_000677.2:n.-35-56C>G
NM_001385624.1:c.-35-56C>G NP_001372553.1:n.-35-56C>G