Canonical Allele Identifier: CA351319869
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs771716822

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878796A>G , CM000664.2:g.240878796A>G GRCh38
NC_000002.11:g.241818213A>G , CM000664.1:g.241818213A>G GRCh37
NC_000002.10:g.241466886A>G NCBI36
NG_008005.1:g.15052A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1154A>G MANE Select ENSP00000302620.3:p.Gln385Arg
ENST00000307503.3:c.1154A>G ENSP00000302620.3:p.Gln385Arg
ENST00000470255.1:n.932A>G
NM_000030.2:c.1154A>G NP_000021.1:p.Gln385Arg
NM_000030.3:c.1154A>G MANE Select NP_000021.1:p.Gln385Arg