Canonical Allele Identifier: CA432021804
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1129557
ClinVar RCV Id: RCV001462766
dbSNP Id: rs2106427613
MyVariant Identifiers: chr2:g.241808697T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869280T>C , CM000664.2:g.240869280T>C GRCh38
NC_000002.11:g.241808697T>C , CM000664.1:g.241808697T>C GRCh37
NC_000002.10:g.241457370T>C NCBI36
NG_008005.1:g.5536T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.276T>C MANE Select ENSP00000302620.3:p.Asn92=
ENST00000307503.3:c.276T>C ENSP00000302620.3:p.Asn92=
ENST00000472436.1:n.296T>C
NM_000030.2:c.276T>C NP_000021.1:p.Asn92=
XR_924060.1:n.405+953A>G
NM_000030.3:c.276T>C MANE Select NP_000021.1:p.Asn92=