Canonical Allele Identifier: CA1339334251
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875263G= , CM000664.2:g.240875263G= GRCh38
NC_000002.11:g.241814680G= , CM000664.1:g.241814680G= GRCh37
NC_000002.10:g.241463353G= NCBI36
NG_008005.1:g.11519G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+59G= MANE Select ENSP00000302620.3:n.776+59G=
ENST00000307503.3:c.776+59G= ENSP00000302620.3:n.776+59G=
ENST00000476698.1:n.428+59G=
NM_000030.2:c.776+59G= NP_000021.1:n.776+59G=
NM_000030.3:c.776+59G= MANE Select NP_000021.1:n.776+59G=