Canonical Allele Identifier: CA2209200
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs756418792

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240875070A>G , CM000664.2:g.240875070A>G GRCh38
NC_000002.11:g.241814487A>G , CM000664.1:g.241814487A>G GRCh37
NC_000002.10:g.241463160A>G NCBI36
NG_008005.1:g.11326A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.681-39A>G MANE Select ENSP00000302620.3:n.681-39A>G
ENST00000307503.3:c.681-39A>G ENSP00000302620.3:n.681-39A>G
ENST00000476698.1:n.333-39A>G
NM_000030.2:c.681-39A>G NP_000021.1:n.681-39A>G
NM_000030.3:c.681-39A>G MANE Select NP_000021.1:n.681-39A>G