Canonical Allele Identifier: CA1339330634
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868687G= , CM000664.2:g.240868687G= GRCh38
NC_000002.11:g.241808104G= , CM000664.1:g.241808104G= GRCh37
NC_000002.10:g.241456777G= NCBI36
NG_008005.1:g.4943G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-179G= ENSP00000302620.3:n.-179G=
XR_924060.1:n.405+1546C=