Canonical Allele Identifier: CA1339333520
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873934C= , CM000664.2:g.240873934C= GRCh38
NC_000002.11:g.241813351C= , CM000664.1:g.241813351C= GRCh37
NC_000002.10:g.241462024C= NCBI36
NG_008005.1:g.10190C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-44C= MANE Select ENSP00000302620.3:n.596-44C=
ENST00000307503.3:c.596-44C= ENSP00000302620.3:n.596-44C=
ENST00000476698.1:n.332+885C=
NM_000030.2:c.596-44C= NP_000021.1:n.596-44C=
NM_000030.3:c.596-44C= MANE Select NP_000021.1:n.596-44C=
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