Canonical Allele Identifier: CA1044064487
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058973983

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868698C>A , CM000664.2:g.240868698C>A GRCh38
NC_000002.11:g.241808115C>A , CM000664.1:g.241808115C>A GRCh37
NC_000002.10:g.241456788C>A NCBI36
NG_008005.1:g.4954C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-168C>A ENSP00000302620.3:n.-168C>A
XR_924060.1:n.405+1535G>T