Canonical Allele Identifier: CA1339336250
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878977C= , CM000664.2:g.240878977C= GRCh38
NC_000002.11:g.241818394C= , CM000664.1:g.241818394C= GRCh37
NC_000002.10:g.241467067C= NCBI36
NG_008005.1:g.15233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*156C= MANE Select ENSP00000302620.3:n.*156C=
ENST00000307503.3:c.*156C= ENSP00000302620.3:n.*156C=
ENST00000470255.1:n.1113C=
NM_000030.2:c.*156C= NP_000021.1:n.*156C=
NM_000030.3:c.*156C= MANE Select NP_000021.1:n.*156C=