Canonical Allele Identifier: CA1339333459
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs1373928663
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873814G>A , CM000664.2:g.240873814G>A GRCh38
NC_000002.11:g.241813231G>A , CM000664.1:g.241813231G>A GRCh37
NC_000002.10:g.241461904G>A NCBI36
NG_008005.1:g.10070G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.596-164G>A MANE Select ENSP00000302620.3:n.596-164G>A
ENST00000307503.3:c.596-164G>A ENSP00000302620.3:n.596-164G>A
ENST00000476698.1:n.332+765G>A
NM_000030.2:c.596-164G>A NP_000021.1:n.596-164G>A
NM_000030.3:c.596-164G>A MANE Select NP_000021.1:n.596-164G>A
Search 100 bp 5'
Search 100 bp 3'