Canonical Allele Identifier: CA2664003989
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868765C>G , CM000664.2:g.240868765C>G GRCh38
NC_000002.11:g.241808182C>G , CM000664.1:g.241808182C>G GRCh37
NC_000002.10:g.241456855C>G NCBI36
NG_008005.1:g.5021C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-101C>G ENSP00000302620.3:n.-101C>G
NM_000030.2:c.-101C>G NP_000021.1:n.-101C>G
XR_924060.1:n.405+1468G>C