Canonical Allele Identifier: CA1339336210
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878890A= , CM000664.2:g.240878890A= GRCh38
NC_000002.11:g.241818307A= , CM000664.1:g.241818307A= GRCh37
NC_000002.10:g.241466980A= NCBI36
NG_008005.1:g.15146A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*69A= MANE Select ENSP00000302620.3:n.*69A=
ENST00000307503.3:c.*69A= ENSP00000302620.3:n.*69A=
ENST00000470255.1:n.1026A=
NM_000030.2:c.*69A= NP_000021.1:n.*69A=
NM_000030.3:c.*69A= MANE Select NP_000021.1:n.*69A=
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