Canonical Allele Identifier: CA1365020070
Gene: ITIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52783581T= , CM000665.2:g.52783581T= GRCh38
NC_000003.11:g.52817597T= , CM000665.1:g.52817597T= GRCh37
NC_000003.10:g.52792637T= NCBI36
NG_016005.1:g.10990T=

Transcript Alleles

HGVS Amino-acid change
ENST00000273283.7:c.1225+242T= MANE Select ENSP00000273283.2:n.1225+242T=
ENST00000273283.6:c.1225+242T= ENSP00000273283.2:n.1225+242T=
ENST00000537050.5:c.361+242T= ENSP00000443847.1:n.361+242T=
ENST00000628722.2:n.1080+242T=
NM_001166434.2:c.799+242T= NP_001159906.1:n.799+242T=
NM_001166435.2:c.361+242T= NP_001159907.1:n.361+242T=
NM_001166436.2:c.361+242T= NP_001159908.1:n.361+242T=
NM_002215.3:c.1225+242T= NP_002206.2:n.1225+242T=
NM_002215.4:c.1225+242T= MANE Select NP_002206.2:n.1225+242T=
NM_001166434.3:c.799+242T= NP_001159906.1:n.799+242T=