Canonical Allele Identifier: CA1339335738
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs2059037233
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878011_240878013del , CM000664.2:g.240878011_240878013del GRCh38
NC_000002.11:g.241817428_241817430del , CM000664.1:g.241817428_241817430del GRCh37
NC_000002.10:g.241466101_241466103del NCBI36
NG_008005.1:g.14267_14269del

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.943-11_943-9del MANE Select ENSP00000302620.3:n.943-11_943-9del
ENST00000307503.3:c.943-11_943-9del ENSP00000302620.3:n.943-11_943-9del
ENST00000470255.1:n.721-11_721-9del
NM_000030.2:c.943-11_943-9del NP_000021.1:n.943-11_943-9del
NM_000030.3:c.943-11_943-9del MANE Select NP_000021.1:n.943-11_943-9del
Search 100 bp 5'
Search 100 bp 3'