Canonical Allele Identifier: CA414339461
Gene: AGTR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.116173220A>C , CM000685.2:g.116173220A>C GRCh38
NC_000023.10:g.115304473A>C , CM000685.1:g.115304473A>C GRCh37
NC_000023.9:g.115218501A>C NCBI36
NG_016326.1:g.7516A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371906.5:c.940A>C MANE Select ENSP00000360973.4:p.Asn314His
ENST00000680409.1:n.1408A>C
ENST00000681852.1:c.940A>C ENSP00000505750.1:p.Asn314His
ENST00000371906.4:c.940A>C ENSP00000360973.4:p.Asn314His
NM_000686.4:c.940A>C NP_000677.2:p.Asn314His
XM_011537533.1:c.940A>C XP_011535835.1:p.Asn314His
NM_000686.5:c.940A>C MANE Select NP_000677.2:p.Asn314His
NM_001385624.1:c.940A>C NP_001372553.1:p.Asn314His