Canonical Allele Identifier: CA2664006402
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873390-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873390C>A , CM000664.2:g.240873390C>A GRCh38
NC_000002.11:g.241812807C>A , CM000664.1:g.241812807C>A GRCh37
NC_000002.10:g.241461480C>A NCBI36
NG_008005.1:g.9646C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+341C>A MANE Select ENSP00000302620.3:n.595+341C>A
ENST00000307503.3:c.595+341C>A ENSP00000302620.3:n.595+341C>A
ENST00000472436.1:n.956C>A
ENST00000476698.1:n.332+341C>A
NM_000030.2:c.595+341C>A NP_000021.1:n.595+341C>A
NM_000030.3:c.595+341C>A MANE Select NP_000021.1:n.595+341C>A
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