Canonical Allele Identifier: CA2694511013
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173606-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173606C>A , CM000685.2:g.116173606C>A GRCh38
NC_000023.10:g.115304859C>A , CM000685.1:g.115304859C>A GRCh37
NC_000023.9:g.115218887C>A NCBI36
NG_016326.1:g.7902C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*234C>A MANE Select ENSP00000360973.4:n.*234C>A
ENST00000371906.4:c.*234C>A ENSP00000360973.4:n.*234C>A
NM_000686.4:c.*234C>A NP_000677.2:n.*234C>A
XM_011537533.1:c.*234C>A XP_011535835.1:n.*234C>A
NM_000686.5:c.*234C>A MANE Select NP_000677.2:n.*234C>A
NM_001385624.1:c.*234C>A NP_001372553.1:n.*234C>A
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