Canonical Allele Identifier: CA2664014000
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879214-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879214A>G , CM000664.2:g.240879214A>G GRCh38
NC_000002.11:g.241818631A>G , CM000664.1:g.241818631A>G GRCh37
NC_000002.10:g.241467304A>G NCBI36
NG_008005.1:g.15470A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*393A>G MANE Select ENSP00000302620.3:n.*393A>G
ENST00000470255.1:n.1350A>G
NM_000030.3:c.*393A>G MANE Select NP_000021.1:n.*393A>G
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