Canonical Allele Identifier: CA351319929
Gene: AGXT HGNC NCBI

Linked Data

gnomAD v4: 2-240878821-A-G
MyVariant Identifiers: chr2:g.241818238A>G (hg19) chr2:g.240878821A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878821A>G , CM000664.2:g.240878821A>G GRCh38
NC_000002.11:g.241818238A>G , CM000664.1:g.241818238A>G GRCh37
NC_000002.10:g.241466911A>G NCBI36
NG_008005.1:g.15077A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.1179A>G MANE Select ENSP00000302620.3:p.Ter393Trp
ENST00000307503.3:c.1179A>G ENSP00000302620.3:p.Ter393Trp
ENST00000470255.1:n.957A>G
NM_000030.2:c.1179A>G NP_000021.1:p.Ter393Trp
NM_000030.3:c.1179A>G MANE Select NP_000021.1:p.Ter393Trp
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