Canonical Allele Identifier: CA1339330592
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868588G= , CM000664.2:g.240868588G= GRCh38
NC_000002.11:g.241808005G= , CM000664.1:g.241808005G= GRCh37
NC_000002.10:g.241456678G= NCBI36
NG_008005.1:g.4844G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-278G= ENSP00000302620.3:n.-278G=
XR_924060.1:n.405+1645C=