Canonical Allele Identifier: CA540538516
Gene: AGXT HGNC NCBI

Linked Data

ClinVar Variation Id: 1091521
ClinVar RCV Id: RCV001411058
dbSNP Id: rs1251940854

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878016C>T , CM000664.2:g.240878016C>T GRCh38
NC_000002.11:g.241817433C>T , CM000664.1:g.241817433C>T GRCh37
NC_000002.10:g.241466106C>T NCBI36
NG_008005.1:g.14272C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-6C>T MANE Select ENSP00000302620.3:n.943-6C>T
ENST00000307503.3:c.943-6C>T ENSP00000302620.3:n.943-6C>T
ENST00000470255.1:n.721-6C>T
NM_000030.2:c.943-6C>T NP_000021.1:n.943-6C>T
NM_000030.3:c.943-6C>T MANE Select NP_000021.1:n.943-6C>T