Canonical Allele Identifier: CA1339333186
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873215A= , CM000664.2:g.240873215A= GRCh38
NC_000002.11:g.241812632A= , CM000664.1:g.241812632A= GRCh37
NC_000002.10:g.241461305A= NCBI36
NG_008005.1:g.9471A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+166A= MANE Select ENSP00000302620.3:n.595+166A=
ENST00000307503.3:c.595+166A= ENSP00000302620.3:n.595+166A=
ENST00000472436.1:n.781A=
ENST00000476698.1:n.332+166A=
NM_000030.2:c.595+166A= NP_000021.1:n.595+166A=
NM_000030.3:c.595+166A= MANE Select NP_000021.1:n.595+166A=