Canonical Allele Identifier: CA1339336296
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879074G= , CM000664.2:g.240879074G= GRCh38
NC_000002.11:g.241818491G= , CM000664.1:g.241818491G= GRCh37
NC_000002.10:g.241467164G= NCBI36
NG_008005.1:g.15330G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*253G= MANE Select ENSP00000302620.3:n.*253G=
ENST00000307503.3:c.*253G= ENSP00000302620.3:n.*253G=
ENST00000470255.1:n.1210G=
NM_000030.2:c.*253G= NP_000021.1:n.*253G=
NM_000030.3:c.*253G= MANE Select NP_000021.1:n.*253G=