Canonical Allele Identifier: CA414339763
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115304605A>G (hg19) chrX:g.116173352A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173352A>G , CM000685.2:g.116173352A>G GRCh38
NC_000023.10:g.115304605A>G , CM000685.1:g.115304605A>G GRCh37
NC_000023.9:g.115218633A>G NCBI36
NG_016326.1:g.7648A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.1072A>G MANE Select ENSP00000360973.4:p.Met358Val
ENST00000680409.1:n.1540A>G
ENST00000681852.1:c.1072A>G ENSP00000505750.1:p.Met358Val
ENST00000371906.4:c.1072A>G ENSP00000360973.4:p.Met358Val
NM_000686.4:c.1072A>G NP_000677.2:p.Met358Val
XM_011537533.1:c.1072A>G XP_011535835.1:p.Met358Val
NM_000686.5:c.1072A>G MANE Select NP_000677.2:p.Met358Val
NM_001385624.1:c.1072A>G NP_001372553.1:p.Met358Val
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