Canonical Allele Identifier: CA2664014001
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879215-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879218del , CM000664.2:g.240879218del GRCh38
NC_000002.11:g.241818635del , CM000664.1:g.241818635del GRCh37
NC_000002.10:g.241467308del NCBI36
NG_008005.1:g.15474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*397del MANE Select ENSP00000302620.3:n.*397del
ENST00000470255.1:n.1354del
NM_000030.3:c.*397del MANE Select NP_000021.1:n.*397del
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