Canonical Allele Identifier: CA2832544652
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873363C>G , CM000664.2:g.240873363C>G GRCh38
NC_000002.11:g.241812780C>G , CM000664.1:g.241812780C>G GRCh37
NC_000002.10:g.241461453C>G NCBI36
NG_008005.1:g.9619C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+314C>G MANE Select ENSP00000302620.3:n.595+314C>G
ENST00000307503.3:c.595+314C>G ENSP00000302620.3:n.595+314C>G
ENST00000472436.1:n.929C>G
ENST00000476698.1:n.332+314C>G
NM_000030.2:c.595+314C>G NP_000021.1:n.595+314C>G
NM_000030.3:c.595+314C>G MANE Select NP_000021.1:n.595+314C>G