Canonical Allele Identifier: CA1339330720
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868853T= , CM000664.2:g.240868853T= GRCh38
NC_000002.11:g.241808270T= , CM000664.1:g.241808270T= GRCh37
NC_000002.10:g.241456943T= NCBI36
NG_008005.1:g.5109T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-13T= MANE Select ENSP00000302620.3:n.-13T=
ENST00000307503.3:c.-13T= ENSP00000302620.3:n.-13T=
ENST00000472436.1:n.8T=
NM_000030.2:c.-13T= NP_000021.1:n.-13T=
XR_924060.1:n.405+1380A=
NM_000030.3:c.-13T= MANE Select NP_000021.1:n.-13T=