Canonical Allele Identifier: CA2664010226

Gene: AGXT

Linked Data

• dbSNP Id: rs2106431405
• gnomAD v4: 2-240877056-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240877056A>G , CM000664.2:g.240877056A>G	GRCh38
NC_000002.11:g.241816473A>G , CM000664.1:g.241816473A>G	GRCh37
NC_000002.10:g.241465146A>G	NCBI36
NG_008005.1:g.13312A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.847-481A>G MANE Select	ENSP00000302620.3:n.847-481A>G
ENST00000307503.3:c.847-481A>G	ENSP00000302620.3:n.847-481A>G
ENST00000470255.1:n.144A>G
NM_000030.2:c.847-481A>G	NP_000021.1:n.847-481A>G
NM_000030.3:c.847-481A>G MANE Select	NP_000021.1:n.847-481A>G