Canonical Allele Identifier: CA1339330737
Gene: AGXT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868877C= , CM000664.2:g.240868877C= GRCh38
NC_000002.11:g.241808294C= , CM000664.1:g.241808294C= GRCh37
NC_000002.10:g.241456967C= NCBI36
NG_008005.1:g.5133C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.12C= MANE Select ENSP00000302620.3:p.His4=
ENST00000307503.3:c.12C= ENSP00000302620.3:p.His4=
ENST00000472436.1:n.32C=
NM_000030.2:c.12C= NP_000021.1:p.His4=
XR_924060.1:n.405+1356G=
NM_000030.3:c.12C= MANE Select NP_000021.1:p.His4=