Canonical Allele Identifier: CA1339330770
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868932C= , CM000664.2:g.240868932C= GRCh38
NC_000002.11:g.241808349C= , CM000664.1:g.241808349C= GRCh37
NC_000002.10:g.241457022C= NCBI36
NG_008005.1:g.5188C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.67C= MANE Select ENSP00000302620.3:p.Gln23=
ENST00000307503.3:c.67C= ENSP00000302620.3:p.Gln23=
ENST00000472436.1:n.87C=
NM_000030.2:c.67C= NP_000021.1:p.Gln23=
XR_924060.1:n.405+1301G=
NM_000030.3:c.67C= MANE Select NP_000021.1:p.Gln23=
Search 100 bp 5'
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