Canonical Allele Identifier: CA1339333076
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873022G= , CM000664.2:g.240873022G= GRCh38
NC_000002.11:g.241812439G= , CM000664.1:g.241812439G= GRCh37
NC_000002.10:g.241461112G= NCBI36
NG_008005.1:g.9278G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.568G= MANE Select ENSP00000302620.3:p.Gly190=
ENST00000307503.3:c.568G= ENSP00000302620.3:p.Gly190=
ENST00000472436.1:n.588G=
ENST00000476698.1:n.305G=
NM_000030.2:c.568G= NP_000021.1:p.Gly190=
NM_000030.3:c.568G= MANE Select NP_000021.1:p.Gly190=