Canonical Allele Identifier: CA1339333529
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873945C= , CM000664.2:g.240873945C= GRCh38
NC_000002.11:g.241813362C= , CM000664.1:g.241813362C= GRCh37
NC_000002.10:g.241462035C= NCBI36
NG_008005.1:g.10201C=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-33C= MANE Select ENSP00000302620.3:n.596-33C=
ENST00000307503.3:c.596-33C= ENSP00000302620.3:n.596-33C=
ENST00000476698.1:n.332+896C=
NM_000030.2:c.596-33C= NP_000021.1:n.596-33C=
NM_000030.3:c.596-33C= MANE Select NP_000021.1:n.596-33C=