Canonical Allele Identifier: CA1339330726
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868861G= , CM000664.2:g.240868861G= GRCh38
NC_000002.11:g.241808278G= , CM000664.1:g.241808278G= GRCh37
NC_000002.10:g.241456951G= NCBI36
NG_008005.1:g.5117G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-5G= MANE Select ENSP00000302620.3:n.-5G=
ENST00000307503.3:c.-5G= ENSP00000302620.3:n.-5G=
ENST00000472436.1:n.16G=
NM_000030.2:c.-5G= NP_000021.1:n.-5G=
XR_924060.1:n.405+1372C=
NM_000030.3:c.-5G= MANE Select NP_000021.1:n.-5G=