Canonical Allele Identifier: CA1339330667
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868749A= , CM000664.2:g.240868749A= GRCh38
NC_000002.11:g.241808166A= , CM000664.1:g.241808166A= GRCh37
NC_000002.10:g.241456839A= NCBI36
NG_008005.1:g.5005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-117A= ENSP00000302620.3:n.-117A=
NM_000030.2:c.-117A= NP_000021.1:n.-117A=
XR_924060.1:n.405+1484T=