Canonical Allele Identifier: CA1339330854
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869081C= , CM000664.2:g.240869081C= GRCh38
NC_000002.11:g.241808498C= , CM000664.1:g.241808498C= GRCh37
NC_000002.10:g.241457171C= NCBI36
NG_008005.1:g.5337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.165+51C= MANE Select ENSP00000302620.3:n.165+51C=
ENST00000307503.3:c.165+51C= ENSP00000302620.3:n.165+51C=
ENST00000472436.1:n.185+51C=
NM_000030.2:c.165+51C= NP_000021.1:n.165+51C=
XR_924060.1:n.405+1152G=
NM_000030.3:c.165+51C= MANE Select NP_000021.1:n.165+51C=
Search 100 bp 5'
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