Canonical Allele Identifier: CA1339333417
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873708G= , CM000664.2:g.240873708G= GRCh38
NC_000002.11:g.241813125G= , CM000664.1:g.241813125G= GRCh37
NC_000002.10:g.241461798G= NCBI36
NG_008005.1:g.9964G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.596-270G= MANE Select ENSP00000302620.3:n.596-270G=
ENST00000307503.3:c.596-270G= ENSP00000302620.3:n.596-270G=
ENST00000476698.1:n.332+659G=
NM_000030.2:c.596-270G= NP_000021.1:n.596-270G=
NM_000030.3:c.596-270G= MANE Select NP_000021.1:n.596-270G=