Canonical Allele Identifier: CA1339330766
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868924T= , CM000664.2:g.240868924T= GRCh38
NC_000002.11:g.241808341T= , CM000664.1:g.241808341T= GRCh37
NC_000002.10:g.241457014T= NCBI36
NG_008005.1:g.5180T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.59T= MANE Select ENSP00000302620.3:p.Ile20=
ENST00000307503.3:c.59T= ENSP00000302620.3:p.Ile20=
ENST00000472436.1:n.79T=
NM_000030.2:c.59T= NP_000021.1:p.Ile20=
XR_924060.1:n.405+1309A=
NM_000030.3:c.59T= MANE Select NP_000021.1:p.Ile20=