Canonical Allele Identifier: CA647781032
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868597T>G , CM000664.2:g.240868597T>G GRCh38
NC_000002.11:g.241808014T>G , CM000664.1:g.241808014T>G GRCh37
NC_000002.10:g.241456687T>G NCBI36
NG_008005.1:g.4853T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-269T>G ENSP00000302620.3:n.-269T>G
XR_924060.1:n.405+1636A>C