Canonical Allele Identifier: CA1339330582
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868570A= , CM000664.2:g.240868570A= GRCh38
NC_000002.11:g.241807987A= , CM000664.1:g.241807987A= GRCh37
NC_000002.10:g.241456660A= NCBI36
NG_008005.1:g.4826A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-296A= ENSP00000302620.3:n.-296A=
XR_924060.1:n.405+1663T=