Canonical Allele Identifier: CA1339336357
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879224G= , CM000664.2:g.240879224G= GRCh38
NC_000002.11:g.241818641G= , CM000664.1:g.241818641G= GRCh37
NC_000002.10:g.241467314G= NCBI36
NG_008005.1:g.15480G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*403G= MANE Select ENSP00000302620.3:n.*403G=
ENST00000470255.1:n.1360G=
NM_000030.3:c.*403G= MANE Select NP_000021.1:n.*403G=