Canonical Allele Identifier: CA2664006352

Gene: AGXT

Linked Data

• dbSNP Id: rs2106429656
• gnomAD v4: 2-240873380-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240873380C>G , CM000664.2:g.240873380C>G	GRCh38
NC_000002.11:g.241812797C>G , CM000664.1:g.241812797C>G	GRCh37
NC_000002.10:g.241461470C>G	NCBI36
NG_008005.1:g.9636C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.595+331C>G MANE Select	ENSP00000302620.3:n.595+331C>G
ENST00000307503.3:c.595+331C>G	ENSP00000302620.3:n.595+331C>G
ENST00000472436.1:n.946C>G
ENST00000476698.1:n.332+331C>G
NM_000030.2:c.595+331C>G	NP_000021.1:n.595+331C>G
NM_000030.3:c.595+331C>G MANE Select	NP_000021.1:n.595+331C>G