Canonical Allele Identifier: CA1339330799
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868988G= , CM000664.2:g.240868988G= GRCh38
NC_000002.11:g.241808405G= , CM000664.1:g.241808405G= GRCh37
NC_000002.10:g.241457078G= NCBI36
NG_008005.1:g.5244G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.123G= MANE Select ENSP00000302620.3:p.Gly41=
ENST00000307503.3:c.123G= ENSP00000302620.3:p.Gly41=
ENST00000472436.1:n.143G=
NM_000030.2:c.123G= NP_000021.1:p.Gly41=
XR_924060.1:n.405+1245C=
NM_000030.3:c.123G= MANE Select NP_000021.1:p.Gly41=