Canonical Allele Identifier: CA2694510838
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116172207-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172207C>G , CM000685.2:g.116172207C>G GRCh38
NC_000023.10:g.115303460C>G , CM000685.1:g.115303460C>G GRCh37
NC_000023.9:g.115217488C>G NCBI36
NG_016326.1:g.6503C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-39C>G MANE Select ENSP00000360973.4:n.-35-39C>G
ENST00000680409.1:n.395C>G
ENST00000681852.1:c.-35-39C>G ENSP00000505750.1:n.-35-39C>G
ENST00000371906.4:c.-35-39C>G ENSP00000360973.4:n.-35-39C>G
NM_000686.4:c.-35-39C>G NP_000677.2:n.-35-39C>G
XM_011537533.1:c.-35-39C>G XP_011535835.1:n.-35-39C>G
NM_000686.5:c.-35-39C>G MANE Select NP_000677.2:n.-35-39C>G
NM_001385624.1:c.-35-39C>G NP_001372553.1:n.-35-39C>G
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