Canonical Allele Identifier: CA2577302551
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240871315-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871315T>G , CM000664.2:g.240871315T>G GRCh38
NC_000002.11:g.241810732T>G , CM000664.1:g.241810732T>G GRCh37
NC_000002.10:g.241459405T>G NCBI36
NG_008005.1:g.7571T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.424-34T>G MANE Select ENSP00000302620.3:n.424-34T>G
ENST00000307503.3:c.424-34T>G ENSP00000302620.3:n.424-34T>G
ENST00000472436.1:n.444-34T>G
ENST00000476698.1:n.127T>G
NM_000030.2:c.424-34T>G NP_000021.1:n.424-34T>G
NM_000030.3:c.424-34T>G MANE Select NP_000021.1:n.424-34T>G
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