Canonical Allele Identifier: CA2577302799
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878871A>G , CM000664.2:g.240878871A>G GRCh38
NC_000002.11:g.241818288A>G , CM000664.1:g.241818288A>G GRCh37
NC_000002.10:g.241466961A>G NCBI36
NG_008005.1:g.15127A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*50A>G MANE Select ENSP00000302620.3:n.*50A>G
ENST00000307503.3:c.*50A>G ENSP00000302620.3:n.*50A>G
ENST00000470255.1:n.1007A>G
NM_000030.2:c.*50A>G NP_000021.1:n.*50A>G
NM_000030.3:c.*50A>G MANE Select NP_000021.1:n.*50A>G