Canonical Allele Identifier: CA414337397
Gene: AGTR2 HGNC NCBI

Linked Data

gnomAD v4: X-116172292-C-G
MyVariant Identifiers: chrX:g.115303545C>G (hg19) chrX:g.116172292C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172292C>G , CM000685.2:g.116172292C>G GRCh38
NC_000023.10:g.115303545C>G , CM000685.1:g.115303545C>G GRCh37
NC_000023.9:g.115217573C>G NCBI36
NG_016326.1:g.6588C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371906.5:c.12C>G MANE Select ENSP00000360973.4:p.Asn4Lys
ENST00000680409.1:n.480C>G
ENST00000681852.1:c.12C>G ENSP00000505750.1:p.Asn4Lys
ENST00000371906.4:c.12C>G ENSP00000360973.4:p.Asn4Lys
NM_000686.4:c.12C>G NP_000677.2:p.Asn4Lys
XM_011537533.1:c.12C>G XP_011535835.1:p.Asn4Lys
NM_000686.5:c.12C>G MANE Select NP_000677.2:p.Asn4Lys
NM_001385624.1:c.12C>G NP_001372553.1:p.Asn4Lys
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