Canonical Allele Identifier: CA1339333267
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873388C= , CM000664.2:g.240873388C= GRCh38
NC_000002.11:g.241812805C= , CM000664.1:g.241812805C= GRCh37
NC_000002.10:g.241461478C= NCBI36
NG_008005.1:g.9644C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+339C= MANE Select ENSP00000302620.3:n.595+339C=
ENST00000307503.3:c.595+339C= ENSP00000302620.3:n.595+339C=
ENST00000472436.1:n.954C=
ENST00000476698.1:n.332+339C=
NM_000030.2:c.595+339C= NP_000021.1:n.595+339C=
NM_000030.3:c.595+339C= MANE Select NP_000021.1:n.595+339C=
Search 100 bp 5'
Search 100 bp 3'