Canonical Allele Identifier: CA1339334147
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875082G= , CM000664.2:g.240875082G= GRCh38
NC_000002.11:g.241814499G= , CM000664.1:g.241814499G= GRCh37
NC_000002.10:g.241463172G= NCBI36
NG_008005.1:g.11338G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-27G= MANE Select ENSP00000302620.3:n.681-27G=
ENST00000307503.3:c.681-27G= ENSP00000302620.3:n.681-27G=
ENST00000476698.1:n.333-27G=
NM_000030.2:c.681-27G= NP_000021.1:n.681-27G=
NM_000030.3:c.681-27G= MANE Select NP_000021.1:n.681-27G=