Canonical Allele Identifier: CA4168733
Gene: AGMO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.15418561T>C , CM000669.2:g.15418561T>C GRCh38
NC_000007.13:g.15458186T>C , CM000669.1:g.15458186T>C GRCh37
NC_000007.12:g.15424711T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001004320.2:c.606A>G MANE Select NP_001004320.1:p.Thr202=
ENST00000342526.8:c.606A>G MANE Select ENSP00000341662.3:p.Thr202=
NM_001004320.1:c.606A>G NP_001004320.1:p.Thr202=
ENST00000342526.7:c.606A>G ENSP00000341662.3:p.Thr202=
XM_006715730.1:c.606A>G XP_006715793.1:p.Thr202=
XM_006715731.2:c.606A>G XP_006715794.1:p.Thr202=
XM_006715731.3:c.606A>G XP_006715794.1:p.Thr202=
XM_011515402.1:c.606A>G XP_011513704.1:p.Thr202=
XM_011515402.3:c.606A>G XP_011513704.1:p.Thr202=
XM_011515403.1:c.606A>G XP_011513705.1:p.Thr202=
XM_017012204.1:c.606A>G XP_016867693.1:p.Thr202=
XR_001744759.1:n.776A>G