Canonical Allele Identifier: CA1339330857
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869085G= , CM000664.2:g.240869085G= GRCh38
NC_000002.11:g.241808502G= , CM000664.1:g.241808502G= GRCh37
NC_000002.10:g.241457175G= NCBI36
NG_008005.1:g.5341G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.165+55G= MANE Select ENSP00000302620.3:n.165+55G=
ENST00000307503.3:c.165+55G= ENSP00000302620.3:n.165+55G=
ENST00000472436.1:n.185+55G=
NM_000030.2:c.165+55G= NP_000021.1:n.165+55G=
XR_924060.1:n.405+1148C=
NM_000030.3:c.165+55G= MANE Select NP_000021.1:n.165+55G=
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