Canonical Allele Identifier: CA1339332195
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871544G= , CM000664.2:g.240871544G= GRCh38
NC_000002.11:g.241810961G= , CM000664.1:g.241810961G= GRCh37
NC_000002.10:g.241459634G= NCBI36
NG_008005.1:g.7800G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.524+95G= MANE Select ENSP00000302620.3:n.524+95G=
ENST00000307503.3:c.524+95G= ENSP00000302620.3:n.524+95G=
ENST00000472436.1:n.544+95G=
ENST00000476698.1:n.261+95G=
NM_000030.2:c.524+95G= NP_000021.1:n.524+95G=
NM_000030.3:c.524+95G= MANE Select NP_000021.1:n.524+95G=
Search 100 bp 5'
Search 100 bp 3'