Canonical Allele Identifier: CA1339331039
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869383G= , CM000664.2:g.240869383G= GRCh38
NC_000002.11:g.241808800G= , CM000664.1:g.241808800G= GRCh37
NC_000002.10:g.241457473G= NCBI36
NG_008005.1:g.5639G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+21G= MANE Select ENSP00000302620.3:n.358+21G=
ENST00000307503.3:c.358+21G= ENSP00000302620.3:n.358+21G=
ENST00000472436.1:n.378+21G=
NM_000030.2:c.358+21G= NP_000021.1:n.358+21G=
XR_924060.1:n.405+850C=
NM_000030.3:c.358+21G= MANE Select NP_000021.1:n.358+21G=