Canonical Allele Identifier: CA2694511001
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173595-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173595C>T , CM000685.2:g.116173595C>T GRCh38
NC_000023.10:g.115304848C>T , CM000685.1:g.115304848C>T GRCh37
NC_000023.9:g.115218876C>T NCBI36
NG_016326.1:g.7891C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*223C>T MANE Select ENSP00000360973.4:n.*223C>T
ENST00000371906.4:c.*223C>T ENSP00000360973.4:n.*223C>T
NM_000686.4:c.*223C>T NP_000677.2:n.*223C>T
XM_011537533.1:c.*223C>T XP_011535835.1:n.*223C>T
NM_000686.5:c.*223C>T MANE Select NP_000677.2:n.*223C>T
NM_001385624.1:c.*223C>T NP_001372553.1:n.*223C>T
Search 100 bp 5'
Search 100 bp 3'