Canonical Allele Identifier: CA1339330682
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868775A= , CM000664.2:g.240868775A= GRCh38
NC_000002.11:g.241808192A= , CM000664.1:g.241808192A= GRCh37
NC_000002.10:g.241456865A= NCBI36
NG_008005.1:g.5031A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-91A= ENSP00000302620.3:n.-91A=
NM_000030.2:c.-91A= NP_000021.1:n.-91A=
XR_924060.1:n.405+1458T=