Canonical Allele Identifier: CA1339336308
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879099G= , CM000664.2:g.240879099G= GRCh38
NC_000002.11:g.241818516G= , CM000664.1:g.241818516G= GRCh37
NC_000002.10:g.241467189G= NCBI36
NG_008005.1:g.15355G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*278G= MANE Select ENSP00000302620.3:n.*278G=
ENST00000307503.3:c.*278G= ENSP00000302620.3:n.*278G=
ENST00000470255.1:n.1235G=
NM_000030.2:c.*278G= NP_000021.1:n.*278G=
NM_000030.3:c.*278G= MANE Select NP_000021.1:n.*278G=