Canonical Allele Identifier: CA1339334184
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875146T= , CM000664.2:g.240875146T= GRCh38
NC_000002.11:g.241814563T= , CM000664.1:g.241814563T= GRCh37
NC_000002.10:g.241463236T= NCBI36
NG_008005.1:g.11402T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.718T= MANE Select ENSP00000302620.3:p.Phe240=
ENST00000307503.3:c.718T= ENSP00000302620.3:p.Phe240=
ENST00000476698.1:n.370T=
NM_000030.2:c.718T= NP_000021.1:p.Phe240=
NM_000030.3:c.718T= MANE Select NP_000021.1:p.Phe240=