Canonical Allele Identifier: CA2664013928
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879183G>A , CM000664.2:g.240879183G>A GRCh38
NC_000002.11:g.241818600G>A , CM000664.1:g.241818600G>A GRCh37
NC_000002.10:g.241467273G>A NCBI36
NG_008005.1:g.15439G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*362G>A MANE Select ENSP00000302620.3:n.*362G>A
ENST00000470255.1:n.1319G>A
NM_000030.3:c.*362G>A MANE Select NP_000021.1:n.*362G>A