Canonical Allele Identifier: CA1339334169
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875121C= , CM000664.2:g.240875121C= GRCh38
NC_000002.11:g.241814538C= , CM000664.1:g.241814538C= GRCh37
NC_000002.10:g.241463211C= NCBI36
NG_008005.1:g.11377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.693C= MANE Select ENSP00000302620.3:p.Tyr231=
ENST00000307503.3:c.693C= ENSP00000302620.3:p.Tyr231=
ENST00000476698.1:n.345C=
NM_000030.2:c.693C= NP_000021.1:p.Tyr231=
NM_000030.3:c.693C= MANE Select NP_000021.1:p.Tyr231=
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