Canonical Allele Identifier: CA1339333148
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873149G= , CM000664.2:g.240873149G= GRCh38
NC_000002.11:g.241812566G= , CM000664.1:g.241812566G= GRCh37
NC_000002.10:g.241461239G= NCBI36
NG_008005.1:g.9405G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+100G= MANE Select ENSP00000302620.3:n.595+100G=
ENST00000307503.3:c.595+100G= ENSP00000302620.3:n.595+100G=
ENST00000472436.1:n.715G=
ENST00000476698.1:n.332+100G=
NM_000030.2:c.595+100G= NP_000021.1:n.595+100G=
NM_000030.3:c.595+100G= MANE Select NP_000021.1:n.595+100G=