Canonical Allele Identifier: CA2664006047
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240873239-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240873239T>G , CM000664.2:g.240873239T>G GRCh38
NC_000002.11:g.241812656T>G , CM000664.1:g.241812656T>G GRCh37
NC_000002.10:g.241461329T>G NCBI36
NG_008005.1:g.9495T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.595+190T>G MANE Select ENSP00000302620.3:n.595+190T>G
ENST00000307503.3:c.595+190T>G ENSP00000302620.3:n.595+190T>G
ENST00000472436.1:n.805T>G
ENST00000476698.1:n.332+190T>G
NM_000030.2:c.595+190T>G NP_000021.1:n.595+190T>G
NM_000030.3:c.595+190T>G MANE Select NP_000021.1:n.595+190T>G
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