Canonical Allele Identifier: CA2694511018
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173614-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173614A>T , CM000685.2:g.116173614A>T GRCh38
NC_000023.10:g.115304867A>T , CM000685.1:g.115304867A>T GRCh37
NC_000023.9:g.115218895A>T NCBI36
NG_016326.1:g.7910A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*242A>T MANE Select ENSP00000360973.4:n.*242A>T
ENST00000371906.4:c.*242A>T ENSP00000360973.4:n.*242A>T
NM_000686.4:c.*242A>T NP_000677.2:n.*242A>T
XM_011537533.1:c.*242A>T XP_011535835.1:n.*242A>T
NM_000686.5:c.*242A>T MANE Select NP_000677.2:n.*242A>T
NM_001385624.1:c.*242A>T NP_001372553.1:n.*242A>T
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