Canonical Allele Identifier: CA1339333554
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873980A= , CM000664.2:g.240873980A= GRCh38
NC_000002.11:g.241813397A= , CM000664.1:g.241813397A= GRCh37
NC_000002.10:g.241462070A= NCBI36
NG_008005.1:g.10236A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.598A= MANE Select ENSP00000302620.3:p.Ile200=
ENST00000307503.3:c.598A= ENSP00000302620.3:p.Ile200=
ENST00000476698.1:n.332+931A=
NM_000030.2:c.598A= NP_000021.1:p.Ile200=
NM_000030.3:c.598A= MANE Select NP_000021.1:p.Ile200=
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