Canonical Allele Identifier: CA432234801
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1576654
ClinVar RCV Id: RCV002078469
dbSNP Id: rs2106427559
MyVariant Identifiers: chr2:g.241808646A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869229A>G , CM000664.2:g.240869229A>G GRCh38
NC_000002.11:g.241808646A>G , CM000664.1:g.241808646A>G GRCh37
NC_000002.10:g.241457319A>G NCBI36
NG_008005.1:g.5485A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.225A>G MANE Select ENSP00000302620.3:p.Thr75=
ENST00000307503.3:c.225A>G ENSP00000302620.3:p.Thr75=
ENST00000472436.1:n.245A>G
NM_000030.2:c.225A>G NP_000021.1:p.Thr75=
XR_924060.1:n.405+1004T>C
NM_000030.3:c.225A>G MANE Select NP_000021.1:p.Thr75=