Canonical Allele Identifier: CA1339330644
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868698C= , CM000664.2:g.240868698C= GRCh38
NC_000002.11:g.241808115C= , CM000664.1:g.241808115C= GRCh37
NC_000002.10:g.241456788C= NCBI36
NG_008005.1:g.4954C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-168C= ENSP00000302620.3:n.-168C=
XR_924060.1:n.405+1535G=