Canonical Allele Identifier: CA2209037
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs752428496

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869227A>G , CM000664.2:g.240869227A>G GRCh38
NC_000002.11:g.241808644A>G , CM000664.1:g.241808644A>G GRCh37
NC_000002.10:g.241457317A>G NCBI36
NG_008005.1:g.5483A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.223A>G MANE Select ENSP00000302620.3:p.Thr75Ala
ENST00000307503.3:c.223A>G ENSP00000302620.3:p.Thr75Ala
ENST00000472436.1:n.243A>G
NM_000030.2:c.223A>G NP_000021.1:p.Thr75Ala
XR_924060.1:n.405+1006T>C
NM_000030.3:c.223A>G MANE Select NP_000021.1:p.Thr75Ala