Canonical Allele Identifier: CA414338085
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116172604-T-G
MyVariant Identifiers: chrX:g.115303857T>G (hg19) chrX:g.116172604T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172604T>G , CM000685.2:g.116172604T>G GRCh38
NC_000023.10:g.115303857T>G , CM000685.1:g.115303857T>G GRCh37
NC_000023.9:g.115217885T>G NCBI36
NG_016326.1:g.6900T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.324T>G MANE Select ENSP00000360973.4:p.Tyr108Ter
ENST00000680409.1:n.792T>G
ENST00000681852.1:c.324T>G ENSP00000505750.1:p.Tyr108Ter
ENST00000371906.4:c.324T>G ENSP00000360973.4:p.Tyr108Ter
NM_000686.4:c.324T>G NP_000677.2:p.Tyr108Ter
XM_011537533.1:c.324T>G XP_011535835.1:p.Tyr108Ter
NM_000686.5:c.324T>G MANE Select NP_000677.2:p.Tyr108Ter
NM_001385624.1:c.324T>G NP_001372553.1:p.Tyr108Ter
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