Canonical Allele Identifier: CA2209173
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs767265467

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873997G>A , CM000664.2:g.240873997G>A GRCh38
NC_000002.11:g.241813414G>A , CM000664.1:g.241813414G>A GRCh37
NC_000002.10:g.241462087G>A NCBI36
NG_008005.1:g.10253G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.615G>A MANE Select ENSP00000302620.3:p.Ser205=
ENST00000307503.3:c.615G>A ENSP00000302620.3:p.Ser205=
ENST00000476698.1:n.332+948G>A
NM_000030.2:c.615G>A NP_000021.1:p.Ser205=
NM_000030.3:c.615G>A MANE Select NP_000021.1:p.Ser205=