Canonical Allele Identifier: CA2694510996
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116173590-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173590T>C , CM000685.2:g.116173590T>C GRCh38
NC_000023.10:g.115304843T>C , CM000685.1:g.115304843T>C GRCh37
NC_000023.9:g.115218871T>C NCBI36
NG_016326.1:g.7886T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.*218T>C MANE Select ENSP00000360973.4:n.*218T>C
ENST00000371906.4:c.*218T>C ENSP00000360973.4:n.*218T>C
NM_000686.4:c.*218T>C NP_000677.2:n.*218T>C
XM_011537533.1:c.*218T>C XP_011535835.1:n.*218T>C
NM_000686.5:c.*218T>C MANE Select NP_000677.2:n.*218T>C
NM_001385624.1:c.*218T>C NP_001372553.1:n.*218T>C
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