Canonical Allele Identifier: CA1339333229
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873311G= , CM000664.2:g.240873311G= GRCh38
NC_000002.11:g.241812728G= , CM000664.1:g.241812728G= GRCh37
NC_000002.10:g.241461401G= NCBI36
NG_008005.1:g.9567G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+262G= MANE Select ENSP00000302620.3:n.595+262G=
ENST00000307503.3:c.595+262G= ENSP00000302620.3:n.595+262G=
ENST00000472436.1:n.877G=
ENST00000476698.1:n.332+262G=
NM_000030.2:c.595+262G= NP_000021.1:n.595+262G=
NM_000030.3:c.595+262G= MANE Select NP_000021.1:n.595+262G=