Canonical Allele Identifier: CA1339336279
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879049A= , CM000664.2:g.240879049A= GRCh38
NC_000002.11:g.241818466A= , CM000664.1:g.241818466A= GRCh37
NC_000002.10:g.241467139A= NCBI36
NG_008005.1:g.15305A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*228A= MANE Select ENSP00000302620.3:n.*228A=
ENST00000307503.3:c.*228A= ENSP00000302620.3:n.*228A=
ENST00000470255.1:n.1185A=
NM_000030.2:c.*228A= NP_000021.1:n.*228A=
NM_000030.3:c.*228A= MANE Select NP_000021.1:n.*228A=