Canonical Allele Identifier: CA1339330697
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058974411

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868817_240868824del , CM000664.2:g.240868817_240868824del GRCh38
NC_000002.11:g.241808234_241808241del , CM000664.1:g.241808234_241808241del GRCh37
NC_000002.10:g.241456907_241456914del NCBI36
NG_008005.1:g.5073_5080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.3:c.-49_-42del ENSP00000302620.3:n.-49_-42del
NM_000030.2:c.-49_-42del NP_000021.1:n.-49_-42del
XR_924060.1:n.405+1409_405+1416del