Canonical Allele Identifier: CA1339330659
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868735A= , CM000664.2:g.240868735A= GRCh38
NC_000002.11:g.241808152A= , CM000664.1:g.241808152A= GRCh37
NC_000002.10:g.241456825A= NCBI36
NG_008005.1:g.4991A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-131A= ENSP00000302620.3:n.-131A=
XR_924060.1:n.405+1498T=