Canonical Allele Identifier: CA2664013948
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240879191-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240879191T>G , CM000664.2:g.240879191T>G GRCh38
NC_000002.11:g.241818608T>G , CM000664.1:g.241818608T>G GRCh37
NC_000002.10:g.241467281T>G NCBI36
NG_008005.1:g.15447T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.*370T>G MANE Select ENSP00000302620.3:n.*370T>G
ENST00000470255.1:n.1327T>G
NM_000030.3:c.*370T>G MANE Select NP_000021.1:n.*370T>G
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