Canonical Allele Identifier: CA1339333593
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240874046T= , CM000664.2:g.240874046T= GRCh38
NC_000002.11:g.241813463T= , CM000664.1:g.241813463T= GRCh37
NC_000002.10:g.241462136T= NCBI36
NG_008005.1:g.10302T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.664T= MANE Select ENSP00000302620.3:p.Phe222=
ENST00000307503.3:c.664T= ENSP00000302620.3:p.Phe222=
ENST00000476698.1:n.332+997T=
NM_000030.2:c.664T= NP_000021.1:p.Phe222=
NM_000030.3:c.664T= MANE Select NP_000021.1:p.Phe222=
Search 100 bp 5'
Search 100 bp 3'