Canonical Allele Identifier: CA1339334314
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875385A= , CM000664.2:g.240875385A= GRCh38
NC_000002.11:g.241814802A= , CM000664.1:g.241814802A= GRCh37
NC_000002.10:g.241463475A= NCBI36
NG_008005.1:g.11641A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+181A= MANE Select ENSP00000302620.3:n.776+181A=
ENST00000307503.3:c.776+181A= ENSP00000302620.3:n.776+181A=
ENST00000476698.1:n.428+181A=
NM_000030.2:c.776+181A= NP_000021.1:n.776+181A=
NM_000030.3:c.776+181A= MANE Select NP_000021.1:n.776+181A=
Search 100 bp 5'
Search 100 bp 3'