Canonical Allele Identifier: CA1365020088
Gene: ITIH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52783615T= , CM000665.2:g.52783615T= GRCh38
NC_000003.11:g.52817631T= , CM000665.1:g.52817631T= GRCh37
NC_000003.10:g.52792671T= NCBI36
NG_016005.1:g.11024T=

Transcript Alleles

HGVS Amino-acid change
ENST00000273283.7:c.1225+276T= MANE Select ENSP00000273283.2:n.1225+276T=
ENST00000273283.6:c.1225+276T= ENSP00000273283.2:n.1225+276T=
ENST00000537050.5:c.361+276T= ENSP00000443847.1:n.361+276T=
ENST00000628722.2:n.1080+276T=
NM_001166434.2:c.799+276T= NP_001159906.1:n.799+276T=
NM_001166435.2:c.361+276T= NP_001159907.1:n.361+276T=
NM_001166436.2:c.361+276T= NP_001159908.1:n.361+276T=
NM_002215.3:c.1225+276T= NP_002206.2:n.1225+276T=
NM_002215.4:c.1225+276T= MANE Select NP_002206.2:n.1225+276T=
NM_001166434.3:c.799+276T= NP_001159906.1:n.799+276T=