Canonical Allele Identifier: CA334723665
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs782693740
MyVariant Identifiers: chrX:g.116171995G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116171995G>T , CM000685.2:g.116171995G>T GRCh38
NC_000023.10:g.115303248G>T , CM000685.1:g.115303248G>T GRCh37
NC_000023.9:g.115217276G>T NCBI36
NG_016326.1:g.6291G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.-35-251G>T MANE Select ENSP00000360973.4:n.-35-251G>T
ENST00000680409.1:n.183G>T
ENST00000681852.1:c.-35-251G>T ENSP00000505750.1:n.-35-251G>T
ENST00000371906.4:c.-35-251G>T ENSP00000360973.4:n.-35-251G>T
NM_000686.4:c.-35-251G>T NP_000677.2:n.-35-251G>T
XM_011537533.1:c.-35-251G>T XP_011535835.1:n.-35-251G>T
NM_000686.5:c.-35-251G>T MANE Select NP_000677.2:n.-35-251G>T
NM_001385624.1:c.-35-251G>T NP_001372553.1:n.-35-251G>T
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