Canonical Allele Identifier: CA353176768
Gene: ITIH3 HGNC NCBI

Linked Data

gnomAD v4: 3-52799401-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52799401T>G , CM000665.2:g.52799401T>G GRCh38
NC_000003.11:g.52833417T>G , CM000665.1:g.52833417T>G GRCh37
NC_000003.10:g.52808457T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000703834.1:c.819T>G ENSP00000515492.1:p.Phe273Leu
ENST00000449956.3:c.819T>G MANE Select ENSP00000415769.2:p.Phe273Leu
ENST00000416872.6:c.819T>G ENSP00000413922.2:p.Phe273Leu
ENST00000449956.2:c.819T>G ENSP00000415769.2:p.Phe273Leu
ENST00000463893.1:n.318T>G
ENST00000465243.6:n.343T>G
ENST00000621946.4:c.819T>G ENSP00000479928.1:p.Phe273Leu
NM_002217.3:c.819T>G NP_002208.3:p.Phe273Leu
XM_005265105.3:c.819T>G XP_005265162.1:p.Phe273Leu
XM_006713129.2:c.819T>G XP_006713192.1:p.Phe273Leu
XM_006713130.2:c.819T>G XP_006713193.1:p.Phe273Leu
XM_005265105.5:c.819T>G XP_005265162.1:p.Phe273Leu
XM_024453512.1:c.-64T>G XP_024309280.1:n.-64T>G
NM_001392019.1:c.819T>G NP_001378948.1:p.Phe273Leu
NM_001392020.1:c.819T>G NP_001378949.1:p.Phe273Leu
NM_001392021.1:c.819T>G NP_001378950.1:p.Phe273Leu
NM_001392022.1:c.819T>G NP_001378951.1:p.Phe273Leu
NM_001392023.1:c.798T>G NP_001378952.1:p.Phe266Leu
NM_001392024.1:c.819T>G NP_001378953.1:p.Phe273Leu
NM_001392025.1:c.819T>G NP_001378954.1:p.Phe273Leu
NM_001392026.1:c.819T>G NP_001378955.1:p.Phe273Leu
NM_001392027.1:c.819T>G NP_001378956.1:p.Phe273Leu
NM_002217.4:c.819T>G MANE Select NP_002208.3:p.Phe273Leu