Canonical Allele Identifier: CA1339334296

Gene: AGXT

Linked Data

• dbSNP Id: rs1575710751

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875350A>G , CM000664.2:g.240875350A>G	GRCh38
NC_000002.11:g.241814767A>G , CM000664.1:g.241814767A>G	GRCh37
NC_000002.10:g.241463440A>G	NCBI36
NG_008005.1:g.11606A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.776+146A>G MANE Select	ENSP00000302620.3:n.776+146A>G
ENST00000307503.3:c.776+146A>G	ENSP00000302620.3:n.776+146A>G
ENST00000476698.1:n.428+146A>G
NM_000030.2:c.776+146A>G	NP_000021.1:n.776+146A>G
NM_000030.3:c.776+146A>G MANE Select	NP_000021.1:n.776+146A>G