Canonical Allele Identifier: CA414337767
Gene: AGTR2 HGNC NCBI

Linked Data

dbSNP Id: rs1602586319
MyVariant Identifiers: chrX:g.115303711C>G (hg19) chrX:g.116172458C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172458C>G , CM000685.2:g.116172458C>G GRCh38
NC_000023.10:g.115303711C>G , CM000685.1:g.115303711C>G GRCh37
NC_000023.9:g.115217739C>G NCBI36
NG_016326.1:g.6754C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.178C>G MANE Select ENSP00000360973.4:p.Leu60Val
ENST00000680409.1:n.646C>G
ENST00000681852.1:c.178C>G ENSP00000505750.1:p.Leu60Val
ENST00000371906.4:c.178C>G ENSP00000360973.4:p.Leu60Val
NM_000686.4:c.178C>G NP_000677.2:p.Leu60Val
XM_011537533.1:c.178C>G XP_011535835.1:p.Leu60Val
NM_000686.5:c.178C>G MANE Select NP_000677.2:p.Leu60Val
NM_001385624.1:c.178C>G NP_001372553.1:p.Leu60Val
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