Canonical Allele Identifier: CA1339331093
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869479G= , CM000664.2:g.240869479G= GRCh38
NC_000002.11:g.241808896G= , CM000664.1:g.241808896G= GRCh37
NC_000002.10:g.241457569G= NCBI36
NG_008005.1:g.5735G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+117G= MANE Select ENSP00000302620.3:n.358+117G=
ENST00000307503.3:c.358+117G= ENSP00000302620.3:n.358+117G=
ENST00000472436.1:n.378+117G=
NM_000030.2:c.358+117G= NP_000021.1:n.358+117G=
XR_924060.1:n.405+754C=
NM_000030.3:c.358+117G= MANE Select NP_000021.1:n.358+117G=
Search 100 bp 5'
Search 100 bp 3'