Canonical Allele Identifier: CA1339336332
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879164C= , CM000664.2:g.240879164C= GRCh38
NC_000002.11:g.241818581C= , CM000664.1:g.241818581C= GRCh37
NC_000002.10:g.241467254C= NCBI36
NG_008005.1:g.15420C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*343C= MANE Select ENSP00000302620.3:n.*343C=
ENST00000470255.1:n.1300C=
NM_000030.3:c.*343C= MANE Select NP_000021.1:n.*343C=