Canonical Allele Identifier: CA2209100
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1136695
ClinVar RCV Id: RCV001472448
dbSNP Id: rs757583201

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871408C>A , CM000664.2:g.240871408C>A GRCh38
NC_000002.11:g.241810825C>A , CM000664.1:g.241810825C>A GRCh37
NC_000002.10:g.241459498C>A NCBI36
NG_008005.1:g.7664C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.483C>A MANE Select ENSP00000302620.3:p.Gly161=
ENST00000307503.3:c.483C>A ENSP00000302620.3:p.Gly161=
ENST00000472436.1:n.503C>A
ENST00000476698.1:n.220C>A
NM_000030.2:c.483C>A NP_000021.1:p.Gly161=
NM_000030.3:c.483C>A MANE Select NP_000021.1:p.Gly161=