Canonical Allele Identifier: CA1339330833
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869050G= , CM000664.2:g.240869050G= GRCh38
NC_000002.11:g.241808467G= , CM000664.1:g.241808467G= GRCh37
NC_000002.10:g.241457140G= NCBI36
NG_008005.1:g.5306G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.165+20G= MANE Select ENSP00000302620.3:n.165+20G=
ENST00000307503.3:c.165+20G= ENSP00000302620.3:n.165+20G=
ENST00000472436.1:n.185+20G=
NM_000030.2:c.165+20G= NP_000021.1:n.165+20G=
XR_924060.1:n.405+1183C=
NM_000030.3:c.165+20G= MANE Select NP_000021.1:n.165+20G=
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