Canonical Allele Identifier: CA1339336349
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879210C= , CM000664.2:g.240879210C= GRCh38
NC_000002.11:g.241818627C= , CM000664.1:g.241818627C= GRCh37
NC_000002.10:g.241467300C= NCBI36
NG_008005.1:g.15466C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*389C= MANE Select ENSP00000302620.3:n.*389C=
ENST00000470255.1:n.1346C=
NM_000030.3:c.*389C= MANE Select NP_000021.1:n.*389C=