Canonical Allele Identifier: CA1365026250
Gene: ITIH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52799071G= , CM000665.2:g.52799071G= GRCh38
NC_000003.11:g.52833087G= , CM000665.1:g.52833087G= GRCh37
NC_000003.10:g.52808127G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703834.1:c.769G= ENSP00000515492.1:p.Glu257=
ENST00000449956.3:c.769G= MANE Select ENSP00000415769.2:p.Glu257=
ENST00000416872.6:c.769G= ENSP00000413922.2:p.Glu257=
ENST00000449956.2:c.769G= ENSP00000415769.2:p.Glu257=
ENST00000463893.1:n.268G=
ENST00000465243.6:n.293G=
ENST00000621946.4:c.769G= ENSP00000479928.1:p.Glu257=
NM_002217.3:c.769G= NP_002208.3:p.Glu257=
XM_005265105.3:c.769G= XP_005265162.1:p.Glu257=
XM_006713129.2:c.769G= XP_006713192.1:p.Glu257=
XM_006713130.2:c.769G= XP_006713193.1:p.Glu257=
XM_005265105.5:c.769G= XP_005265162.1:p.Glu257=
XM_024453512.1:c.-114G= XP_024309280.1:n.-114G=
NM_001392019.1:c.769G= NP_001378948.1:p.Glu257=
NM_001392020.1:c.769G= NP_001378949.1:p.Glu257=
NM_001392021.1:c.769G= NP_001378950.1:p.Glu257=
NM_001392022.1:c.769G= NP_001378951.1:p.Glu257=
NM_001392023.1:c.748G= NP_001378952.1:p.Glu250=
NM_001392024.1:c.769G= NP_001378953.1:p.Glu257=
NM_001392025.1:c.769G= NP_001378954.1:p.Glu257=
NM_001392026.1:c.769G= NP_001378955.1:p.Glu257=
NM_001392027.1:c.769G= NP_001378956.1:p.Glu257=
NM_002217.4:c.769G= MANE Select NP_002208.3:p.Glu257=