Canonical Allele Identifier: CA2664011486
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240877881-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240877881T>G , CM000664.2:g.240877881T>G GRCh38
NC_000002.11:g.241817298T>G , CM000664.1:g.241817298T>G GRCh37
NC_000002.10:g.241465971T>G NCBI36
NG_008005.1:g.14137T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.943-141T>G MANE Select ENSP00000302620.3:n.943-141T>G
ENST00000307503.3:c.943-141T>G ENSP00000302620.3:n.943-141T>G
ENST00000470255.1:n.721-141T>G
NM_000030.2:c.943-141T>G NP_000021.1:n.943-141T>G
NM_000030.3:c.943-141T>G MANE Select NP_000021.1:n.943-141T>G
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