Canonical Allele Identifier: CA1339336117
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240878714G= , CM000664.2:g.240878714G= GRCh38
NC_000002.11:g.241818131G= , CM000664.1:g.241818131G= GRCh37
NC_000002.10:g.241466804G= NCBI36
NG_008005.1:g.14970G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307503.4:c.1072G= MANE Select ENSP00000302620.3:p.Val358=
ENST00000307503.3:c.1072G= ENSP00000302620.3:p.Val358=
ENST00000470255.1:n.850G=
NM_000030.2:c.1072G= NP_000021.1:p.Val358=
NM_000030.3:c.1072G= MANE Select NP_000021.1:p.Val358=