Canonical Allele Identifier: CA351313808
Gene: AGXT HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.241808735A>T (hg19) chr2:g.240869318A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869318A>T , CM000664.2:g.240869318A>T GRCh38
NC_000002.11:g.241808735A>T , CM000664.1:g.241808735A>T GRCh37
NC_000002.10:g.241457408A>T NCBI36
NG_008005.1:g.5574A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.314A>T MANE Select ENSP00000302620.3:p.Asn105Ile
ENST00000307503.3:c.314A>T ENSP00000302620.3:p.Asn105Ile
ENST00000472436.1:n.334A>T
NM_000030.2:c.314A>T NP_000021.1:p.Asn105Ile
XR_924060.1:n.405+915T>A
NM_000030.3:c.314A>T MANE Select NP_000021.1:p.Asn105Ile
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