Canonical Allele Identifier: CA414337839
Gene: AGTR2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.115303745G>T (hg19) chrX:g.116172492G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172492G>T , CM000685.2:g.116172492G>T GRCh38
NC_000023.10:g.115303745G>T , CM000685.1:g.115303745G>T GRCh37
NC_000023.9:g.115217773G>T NCBI36
NG_016326.1:g.6788G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.212G>T MANE Select ENSP00000360973.4:p.Cys71Phe
ENST00000680409.1:n.680G>T
ENST00000681852.1:c.212G>T ENSP00000505750.1:p.Cys71Phe
ENST00000371906.4:c.212G>T ENSP00000360973.4:p.Cys71Phe
NM_000686.4:c.212G>T NP_000677.2:p.Cys71Phe
XM_011537533.1:c.212G>T XP_011535835.1:p.Cys71Phe
NM_000686.5:c.212G>T MANE Select NP_000677.2:p.Cys71Phe
NM_001385624.1:c.212G>T NP_001372553.1:p.Cys71Phe
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