Canonical Allele Identifier: CA1339330946
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869227A= , CM000664.2:g.240869227A= GRCh38
NC_000002.11:g.241808644A= , CM000664.1:g.241808644A= GRCh37
NC_000002.10:g.241457317A= NCBI36
NG_008005.1:g.5483A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.223A= MANE Select ENSP00000302620.3:p.Thr75=
ENST00000307503.3:c.223A= ENSP00000302620.3:p.Thr75=
ENST00000472436.1:n.243A=
NM_000030.2:c.223A= NP_000021.1:p.Thr75=
XR_924060.1:n.405+1006T=
NM_000030.3:c.223A= MANE Select NP_000021.1:p.Thr75=