Canonical Allele Identifier: CA1339334322
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059018688
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875396G>A , CM000664.2:g.240875396G>A GRCh38
NC_000002.11:g.241814813G>A , CM000664.1:g.241814813G>A GRCh37
NC_000002.10:g.241463486G>A NCBI36
NG_008005.1:g.11652G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.776+192G>A MANE Select ENSP00000302620.3:n.776+192G>A
ENST00000307503.3:c.776+192G>A ENSP00000302620.3:n.776+192G>A
ENST00000476698.1:n.428+192G>A
NM_000030.2:c.776+192G>A NP_000021.1:n.776+192G>A
NM_000030.3:c.776+192G>A MANE Select NP_000021.1:n.776+192G>A
Search 100 bp 5'
Search 100 bp 3'