Canonical Allele Identifier: CA1339330903
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869137G= , CM000664.2:g.240869137G= GRCh38
NC_000002.11:g.241808554G= , CM000664.1:g.241808554G= GRCh37
NC_000002.10:g.241457227G= NCBI36
NG_008005.1:g.5393G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.166-33G= MANE Select ENSP00000302620.3:n.166-33G=
ENST00000307503.3:c.166-33G= ENSP00000302620.3:n.166-33G=
ENST00000472436.1:n.186-33G=
NM_000030.2:c.166-33G= NP_000021.1:n.166-33G=
XR_924060.1:n.405+1096C=
NM_000030.3:c.166-33G= MANE Select NP_000021.1:n.166-33G=