Canonical Allele Identifier: CA1339330606
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058973638

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868624del , CM000664.2:g.240868624del GRCh38
NC_000002.11:g.241808041del , CM000664.1:g.241808041del GRCh37
NC_000002.10:g.241456714del NCBI36
NG_008005.1:g.4880del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-242del ENSP00000302620.3:n.-242del
XR_924060.1:n.405+1609del