Canonical Allele Identifier: CA1339336350
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879212G= , CM000664.2:g.240879212G= GRCh38
NC_000002.11:g.241818629G= , CM000664.1:g.241818629G= GRCh37
NC_000002.10:g.241467302G= NCBI36
NG_008005.1:g.15468G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*391G= MANE Select ENSP00000302620.3:n.*391G=
ENST00000470255.1:n.1348G=
NM_000030.3:c.*391G= MANE Select NP_000021.1:n.*391G=
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