Canonical Allele Identifier: CA2664010850
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877360T>G , CM000664.2:g.240877360T>G GRCh38
NC_000002.11:g.241816777T>G , CM000664.1:g.241816777T>G GRCh37
NC_000002.10:g.241465450T>G NCBI36
NG_008005.1:g.13616T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.847-177T>G MANE Select ENSP00000302620.3:n.847-177T>G
ENST00000307503.3:c.847-177T>G ENSP00000302620.3:n.847-177T>G
ENST00000470255.1:n.448T>G
NM_000030.2:c.847-177T>G NP_000021.1:n.847-177T>G
NM_000030.3:c.847-177T>G MANE Select NP_000021.1:n.847-177T>G