Canonical Allele Identifier: CA2209050
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs180177203

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869336G>T , CM000664.2:g.240869336G>T GRCh38
NC_000002.11:g.241808753G>T , CM000664.1:g.241808753G>T GRCh37
NC_000002.10:g.241457426G>T NCBI36
NG_008005.1:g.5592G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.332G>T MANE Select ENSP00000302620.3:p.Arg111Leu
ENST00000307503.3:c.332G>T ENSP00000302620.3:p.Arg111Leu
ENST00000472436.1:n.352G>T
NM_000030.2:c.332G>T NP_000021.1:p.Arg111Leu
XR_924060.1:n.405+897C>A
NM_000030.3:c.332G>T MANE Select NP_000021.1:p.Arg111Leu