Canonical Allele Identifier: CA1365020096
Gene: ITIH1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52783630C= , CM000665.2:g.52783630C= GRCh38
NC_000003.11:g.52817646C= , CM000665.1:g.52817646C= GRCh37
NC_000003.10:g.52792686C= NCBI36
NG_016005.1:g.11039C=

Transcript Alleles

HGVS Amino-acid change
ENST00000273283.7:c.1225+291C= MANE Select ENSP00000273283.2:n.1225+291C=
ENST00000273283.6:c.1225+291C= ENSP00000273283.2:n.1225+291C=
ENST00000537050.5:c.361+291C= ENSP00000443847.1:n.361+291C=
ENST00000628722.2:n.1080+291C=
NM_001166434.2:c.799+291C= NP_001159906.1:n.799+291C=
NM_001166435.2:c.361+291C= NP_001159907.1:n.361+291C=
NM_001166436.2:c.361+291C= NP_001159908.1:n.361+291C=
NM_002215.3:c.1225+291C= NP_002206.2:n.1225+291C=
NM_002215.4:c.1225+291C= MANE Select NP_002206.2:n.1225+291C=
NM_001166434.3:c.799+291C= NP_001159906.1:n.799+291C=
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