Canonical Allele Identifier: CA2664012698
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878843-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878843G>A , CM000664.2:g.240878843G>A GRCh38
NC_000002.11:g.241818260G>A , CM000664.1:g.241818260G>A GRCh37
NC_000002.10:g.241466933G>A NCBI36
NG_008005.1:g.15099G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*22G>A MANE Select ENSP00000302620.3:n.*22G>A
ENST00000307503.3:c.*22G>A ENSP00000302620.3:n.*22G>A
ENST00000470255.1:n.979G>A
NM_000030.2:c.*22G>A NP_000021.1:n.*22G>A
NM_000030.3:c.*22G>A MANE Select NP_000021.1:n.*22G>A
Search 100 bp 5'
Search 100 bp 3'