Canonical Allele Identifier: CA1339334287
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875334C= , CM000664.2:g.240875334C= GRCh38
NC_000002.11:g.241814751C= , CM000664.1:g.241814751C= GRCh37
NC_000002.10:g.241463424C= NCBI36
NG_008005.1:g.11590C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+130C= MANE Select ENSP00000302620.3:n.776+130C=
ENST00000307503.3:c.776+130C= ENSP00000302620.3:n.776+130C=
ENST00000476698.1:n.428+130C=
NM_000030.2:c.776+130C= NP_000021.1:n.776+130C=
NM_000030.3:c.776+130C= MANE Select NP_000021.1:n.776+130C=