Canonical Allele Identifier: CA1339331066
Gene: AGXT HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869440G= , CM000664.2:g.240869440G= GRCh38
NC_000002.11:g.241808857G= , CM000664.1:g.241808857G= GRCh37
NC_000002.10:g.241457530G= NCBI36
NG_008005.1:g.5696G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+78G= MANE Select ENSP00000302620.3:n.358+78G=
ENST00000307503.3:c.358+78G= ENSP00000302620.3:n.358+78G=
ENST00000472436.1:n.378+78G=
NM_000030.2:c.358+78G= NP_000021.1:n.358+78G=
XR_924060.1:n.405+793C=
NM_000030.3:c.358+78G= MANE Select NP_000021.1:n.358+78G=
Search 100 bp 5'
Search 100 bp 3'