Canonical Allele Identifier: CA2664006320
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873373T>G , CM000664.2:g.240873373T>G GRCh38
NC_000002.11:g.241812790T>G , CM000664.1:g.241812790T>G GRCh37
NC_000002.10:g.241461463T>G NCBI36
NG_008005.1:g.9629T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+324T>G MANE Select ENSP00000302620.3:n.595+324T>G
ENST00000307503.3:c.595+324T>G ENSP00000302620.3:n.595+324T>G
ENST00000472436.1:n.939T>G
ENST00000476698.1:n.332+324T>G
NM_000030.2:c.595+324T>G NP_000021.1:n.595+324T>G
NM_000030.3:c.595+324T>G MANE Select NP_000021.1:n.595+324T>G