Canonical Allele Identifier: CA1339330551
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868501G= , CM000664.2:g.240868501G= GRCh38
NC_000002.11:g.241807918G= , CM000664.1:g.241807918G= GRCh37
NC_000002.10:g.241456591G= NCBI36
NG_008005.1:g.4757G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-365G= ENSP00000302620.3:n.-365G=
XR_924060.1:n.405+1732C=