Canonical Allele Identifier: CA1339335663
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877868G= , CM000664.2:g.240877868G= GRCh38
NC_000002.11:g.241817285G= , CM000664.1:g.241817285G= GRCh37
NC_000002.10:g.241465958G= NCBI36
NG_008005.1:g.14124G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-154G= MANE Select ENSP00000302620.3:n.943-154G=
ENST00000307503.3:c.943-154G= ENSP00000302620.3:n.943-154G=
ENST00000470255.1:n.721-154G=
NM_000030.2:c.943-154G= NP_000021.1:n.943-154G=
NM_000030.3:c.943-154G= MANE Select NP_000021.1:n.943-154G=
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