Canonical Allele Identifier: CA1339336358
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879225T= , CM000664.2:g.240879225T= GRCh38
NC_000002.11:g.241818642T= , CM000664.1:g.241818642T= GRCh37
NC_000002.10:g.241467315T= NCBI36
NG_008005.1:g.15481T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*404T= MANE Select ENSP00000302620.3:n.*404T=
ENST00000470255.1:n.1361T=
NM_000030.3:c.*404T= MANE Select NP_000021.1:n.*404T=