Canonical Allele Identifier: CA1339334162
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875106C= , CM000664.2:g.240875106C= GRCh38
NC_000002.11:g.241814523C= , CM000664.1:g.241814523C= GRCh37
NC_000002.10:g.241463196C= NCBI36
NG_008005.1:g.11362C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-3C= MANE Select ENSP00000302620.3:n.681-3C=
ENST00000307503.3:c.681-3C= ENSP00000302620.3:n.681-3C=
ENST00000476698.1:n.333-3C=
NM_000030.2:c.681-3C= NP_000021.1:n.681-3C=
NM_000030.3:c.681-3C= MANE Select NP_000021.1:n.681-3C=
Search 100 bp 5'
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