Canonical Allele Identifier: CA1339330638
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868691T= , CM000664.2:g.240868691T= GRCh38
NC_000002.11:g.241808108T= , CM000664.1:g.241808108T= GRCh37
NC_000002.10:g.241456781T= NCBI36
NG_008005.1:g.4947T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-175T= ENSP00000302620.3:n.-175T=
XR_924060.1:n.405+1542A=