Canonical Allele Identifier: CA432021838
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 2912007
ClinVar RCV Id: RCV003738707
dbSNP Id: rs2058978609
MyVariant Identifiers: chr2:g.241808703G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869286G>A , CM000664.2:g.240869286G>A GRCh38
NC_000002.11:g.241808703G>A , CM000664.1:g.241808703G>A GRCh37
NC_000002.10:g.241457376G>A NCBI36
NG_008005.1:g.5542G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.282G>A MANE Select ENSP00000302620.3:p.Leu94=
ENST00000307503.3:c.282G>A ENSP00000302620.3:p.Leu94=
ENST00000472436.1:n.302G>A
NM_000030.2:c.282G>A NP_000021.1:p.Leu94=
XR_924060.1:n.405+947C>T
NM_000030.3:c.282G>A MANE Select NP_000021.1:p.Leu94=