Canonical Allele Identifier: CA1339330687
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868782T= , CM000664.2:g.240868782T= GRCh38
NC_000002.11:g.241808199T= , CM000664.1:g.241808199T= GRCh37
NC_000002.10:g.241456872T= NCBI36
NG_008005.1:g.5038T=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-84T= ENSP00000302620.3:n.-84T=
NM_000030.2:c.-84T= NP_000021.1:n.-84T=
XR_924060.1:n.405+1451A=