Canonical Allele Identifier: CA2209102
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 898218
ClinVar RCV Id: RCV001141971
dbSNP Id: rs528938116

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871416A>T , CM000664.2:g.240871416A>T GRCh38
NC_000002.11:g.241810833A>T , CM000664.1:g.241810833A>T GRCh37
NC_000002.10:g.241459506A>T NCBI36
NG_008005.1:g.7672A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.491A>T MANE Select ENSP00000302620.3:p.Gln164Leu
ENST00000307503.3:c.491A>T ENSP00000302620.3:p.Gln164Leu
ENST00000472436.1:n.511A>T
ENST00000476698.1:n.228A>T
NM_000030.2:c.491A>T NP_000021.1:p.Gln164Leu
NM_000030.3:c.491A>T MANE Select NP_000021.1:p.Gln164Leu