Canonical Allele Identifier: CA1339335712

Gene: AGXT

Linked Data

• dbSNP Id: rs2059036864
• gnomAD v4: 2-240877970-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877970A>G , CM000664.2:g.240877970A>G	GRCh38
NC_000002.11:g.241817387A>G , CM000664.1:g.241817387A>G	GRCh37
NC_000002.10:g.241466060A>G	NCBI36
NG_008005.1:g.14226A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.943-52A>G MANE Select	ENSP00000302620.3:n.943-52A>G
ENST00000307503.3:c.943-52A>G	ENSP00000302620.3:n.943-52A>G
ENST00000470255.1:n.721-52A>G
NM_000030.2:c.943-52A>G	NP_000021.1:n.943-52A>G
NM_000030.3:c.943-52A>G MANE Select	NP_000021.1:n.943-52A>G