Canonical Allele Identifier: CA2664003642
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2106427148

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868667G>A , CM000664.2:g.240868667G>A GRCh38
NC_000002.11:g.241808084G>A , CM000664.1:g.241808084G>A GRCh37
NC_000002.10:g.241456757G>A NCBI36
NG_008005.1:g.4923G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-199G>A ENSP00000302620.3:n.-199G>A
XR_924060.1:n.405+1566C>T