Canonical Allele Identifier: CA68178394
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs757583201

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871408C>T , CM000664.2:g.240871408C>T GRCh38
NC_000002.11:g.241810825C>T , CM000664.1:g.241810825C>T GRCh37
NC_000002.10:g.241459498C>T NCBI36
NG_008005.1:g.7664C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.483C>T MANE Select ENSP00000302620.3:p.Gly161=
ENST00000307503.3:c.483C>T ENSP00000302620.3:p.Gly161=
ENST00000472436.1:n.503C>T
ENST00000476698.1:n.220C>T
NM_000030.2:c.483C>T NP_000021.1:p.Gly161=
NM_000030.3:c.483C>T MANE Select NP_000021.1:p.Gly161=