Canonical Allele Identifier: CA414337576
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116172371T>G , CM000685.2:g.116172371T>G GRCh38
NC_000023.10:g.115303624T>G , CM000685.1:g.115303624T>G GRCh37
NC_000023.9:g.115217652T>G NCBI36
NG_016326.1:g.6667T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.91T>G MANE Select ENSP00000360973.4:p.Ser31Ala
ENST00000680409.1:n.559T>G
ENST00000681852.1:c.91T>G ENSP00000505750.1:p.Ser31Ala
ENST00000371906.4:c.91T>G ENSP00000360973.4:p.Ser31Ala
NM_000686.4:c.91T>G NP_000677.2:p.Ser31Ala
XM_011537533.1:c.91T>G XP_011535835.1:p.Ser31Ala
NM_000686.5:c.91T>G MANE Select NP_000677.2:p.Ser31Ala
NM_001385624.1:c.91T>G NP_001372553.1:p.Ser31Ala