Canonical Allele Identifier: CA1044064512
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2058974272

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868775_240868777del , CM000664.2:g.240868775_240868777del GRCh38
NC_000002.11:g.241808192_241808194del , CM000664.1:g.241808192_241808194del GRCh37
NC_000002.10:g.241456865_241456867del NCBI36
NG_008005.1:g.5031_5033del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.3:c.-91_-89del ENSP00000302620.3:n.-91_-89del
NM_000030.2:c.-91_-89del NP_000021.1:n.-91_-89del
XR_924060.1:n.405+1457_405+1459del