Canonical Allele Identifier: CA1339330689
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868787G= , CM000664.2:g.240868787G= GRCh38
NC_000002.11:g.241808204G= , CM000664.1:g.241808204G= GRCh37
NC_000002.10:g.241456877G= NCBI36
NG_008005.1:g.5043G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-79G= ENSP00000302620.3:n.-79G=
NM_000030.2:c.-79G= NP_000021.1:n.-79G=
XR_924060.1:n.405+1446C=