Canonical Allele Identifier: CA1339336304
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879087A= , CM000664.2:g.240879087A= GRCh38
NC_000002.11:g.241818504A= , CM000664.1:g.241818504A= GRCh37
NC_000002.10:g.241467177A= NCBI36
NG_008005.1:g.15343A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*266A= MANE Select ENSP00000302620.3:n.*266A=
ENST00000307503.3:c.*266A= ENSP00000302620.3:n.*266A=
ENST00000470255.1:n.1223A=
NM_000030.2:c.*266A= NP_000021.1:n.*266A=
NM_000030.3:c.*266A= MANE Select NP_000021.1:n.*266A=