Canonical Allele Identifier: CA334723700
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs34589510

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173429dup , CM000685.2:g.116173429dup GRCh38
NC_000023.10:g.115304682dup , CM000685.1:g.115304682dup GRCh37
NC_000023.9:g.115218710dup NCBI36
NG_016326.1:g.7725dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*57dup MANE Select ENSP00000360973.4:n.*57dup
ENST00000680409.1:n.1617dup
ENST00000371906.4:c.*57dup ENSP00000360973.4:n.*57dup
NM_000686.4:c.*57dup NP_000677.2:n.*57dup
XM_011537533.1:c.*57dup XP_011535835.1:n.*57dup
NM_000686.5:c.*57dup MANE Select NP_000677.2:n.*57dup
NM_001385624.1:c.*57dup NP_001372553.1:n.*57dup