Canonical Allele Identifier: CA68173646
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs368944802

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869106del , CM000664.2:g.240869106del GRCh38
NC_000002.11:g.241808523del , CM000664.1:g.241808523del GRCh37
NC_000002.10:g.241457196del NCBI36
NG_008005.1:g.5362del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.166-64del MANE Select ENSP00000302620.3:n.166-64del
ENST00000307503.3:c.166-64del ENSP00000302620.3:n.166-64del
ENST00000472436.1:n.186-64del
NM_000030.2:c.166-64del NP_000021.1:n.166-64del
XR_924060.1:n.405+1131del
NM_000030.3:c.166-64del MANE Select NP_000021.1:n.166-64del