Canonical Allele Identifier: CA1339335709
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877967A= , CM000664.2:g.240877967A= GRCh38
NC_000002.11:g.241817384A= , CM000664.1:g.241817384A= GRCh37
NC_000002.10:g.241466057A= NCBI36
NG_008005.1:g.14223A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-55A= MANE Select ENSP00000302620.3:n.943-55A=
ENST00000307503.3:c.943-55A= ENSP00000302620.3:n.943-55A=
ENST00000470255.1:n.721-55A=
NM_000030.2:c.943-55A= NP_000021.1:n.943-55A=
NM_000030.3:c.943-55A= MANE Select NP_000021.1:n.943-55A=
Search 100 bp 5'
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