Canonical Allele Identifier: CA2664006297

Gene: AGXT

Linked Data

• gnomAD v4: 2-240873367-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873367C>G , CM000664.2:g.240873367C>G	GRCh38
NC_000002.11:g.241812784C>G , CM000664.1:g.241812784C>G	GRCh37
NC_000002.10:g.241461457C>G	NCBI36
NG_008005.1:g.9623C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.595+318C>G MANE Select	ENSP00000302620.3:n.595+318C>G
ENST00000307503.3:c.595+318C>G	ENSP00000302620.3:n.595+318C>G
ENST00000472436.1:n.933C>G
ENST00000476698.1:n.332+318C>G
NM_000030.2:c.595+318C>G	NP_000021.1:n.595+318C>G
NM_000030.3:c.595+318C>G MANE Select	NP_000021.1:n.595+318C>G