Canonical Allele Identifier: CA1339332080
Gene: AGXT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240871360G= , CM000664.2:g.240871360G= GRCh38
NC_000002.11:g.241810777G= , CM000664.1:g.241810777G= GRCh37
NC_000002.10:g.241459450G= NCBI36
NG_008005.1:g.7616G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.435G= MANE Select ENSP00000302620.3:p.Gln145=
ENST00000307503.3:c.435G= ENSP00000302620.3:p.Gln145=
ENST00000472436.1:n.455G=
ENST00000476698.1:n.172G=
NM_000030.2:c.435G= NP_000021.1:p.Gln145=
NM_000030.3:c.435G= MANE Select NP_000021.1:p.Gln145=
Search 100 bp 5'
Search 100 bp 3'