Canonical Allele Identifier: CA68173832
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1148003
ClinVar RCV Id: RCV001487725
dbSNP Id: rs917296853

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869277C>T , CM000664.2:g.240869277C>T GRCh38
NC_000002.11:g.241808694C>T , CM000664.1:g.241808694C>T GRCh37
NC_000002.10:g.241457367C>T NCBI36
NG_008005.1:g.5533C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.273C>T MANE Select ENSP00000302620.3:p.Val91=
ENST00000307503.3:c.273C>T ENSP00000302620.3:p.Val91=
ENST00000472436.1:n.293C>T
NM_000030.2:c.273C>T NP_000021.1:p.Val91=
XR_924060.1:n.405+956G>A
NM_000030.3:c.273C>T MANE Select NP_000021.1:p.Val91=