Canonical Allele Identifier: CA1339334174
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875127C= , CM000664.2:g.240875127C= GRCh38
NC_000002.11:g.241814544C= , CM000664.1:g.241814544C= GRCh37
NC_000002.10:g.241463217C= NCBI36
NG_008005.1:g.11383C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.699C= MANE Select ENSP00000302620.3:p.Arg233=
ENST00000307503.3:c.699C= ENSP00000302620.3:p.Arg233=
ENST00000476698.1:n.351C=
NM_000030.2:c.699C= NP_000021.1:p.Arg233=
NM_000030.3:c.699C= MANE Select NP_000021.1:p.Arg233=