Canonical Allele Identifier: CA1339333152
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873153T= , CM000664.2:g.240873153T= GRCh38
NC_000002.11:g.241812570T= , CM000664.1:g.241812570T= GRCh37
NC_000002.10:g.241461243T= NCBI36
NG_008005.1:g.9409T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+104T= MANE Select ENSP00000302620.3:n.595+104T=
ENST00000307503.3:c.595+104T= ENSP00000302620.3:n.595+104T=
ENST00000472436.1:n.719T=
ENST00000476698.1:n.332+104T=
NM_000030.2:c.595+104T= NP_000021.1:n.595+104T=
NM_000030.3:c.595+104T= MANE Select NP_000021.1:n.595+104T=