Canonical Allele Identifier: CA1339332058
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871320T= , CM000664.2:g.240871320T= GRCh38
NC_000002.11:g.241810737T= , CM000664.1:g.241810737T= GRCh37
NC_000002.10:g.241459410T= NCBI36
NG_008005.1:g.7576T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.424-29T= MANE Select ENSP00000302620.3:n.424-29T=
ENST00000307503.3:c.424-29T= ENSP00000302620.3:n.424-29T=
ENST00000472436.1:n.444-29T=
ENST00000476698.1:n.132T=
NM_000030.2:c.424-29T= NP_000021.1:n.424-29T=
NM_000030.3:c.424-29T= MANE Select NP_000021.1:n.424-29T=
Search 100 bp 5'
Search 100 bp 3'