Canonical Allele Identifier: CA1339335774
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878066C= , CM000664.2:g.240878066C= GRCh38
NC_000002.11:g.241817483C= , CM000664.1:g.241817483C= GRCh37
NC_000002.10:g.241466156C= NCBI36
NG_008005.1:g.14322C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.987C= MANE Select ENSP00000302620.3:p.Gly329=
ENST00000307503.3:c.987C= ENSP00000302620.3:p.Gly329=
ENST00000470255.1:n.765C=
NM_000030.2:c.987C= NP_000021.1:p.Gly329=
NM_000030.3:c.987C= MANE Select NP_000021.1:p.Gly329=
Search 100 bp 5'
Search 100 bp 3'