Canonical Allele Identifier: CA1047982009
Gene: ITIH1 HGNC NCBI

Linked Data

dbSNP Id: rs1699214742
gnomAD v3: 3-52786825-T-G
gnomAD v4: 3-52786825-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52786825T>G , CM000665.2:g.52786825T>G GRCh38
NC_000003.11:g.52820841T>G , CM000665.1:g.52820841T>G GRCh37
NC_000003.10:g.52795881T>G NCBI36
NG_016005.1:g.14234T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000273283.7:c.1734-120T>G MANE Select ENSP00000273283.2:n.1734-120T>G
ENST00000273283.6:c.1734-120T>G ENSP00000273283.2:n.1734-120T>G
ENST00000428133.5:c.393-120T>G ENSP00000395836.1:n.393-120T>G
ENST00000537050.5:c.870-120T>G ENSP00000443847.1:n.870-120T>G
ENST00000628722.2:n.1589-120T>G
NM_001166434.2:c.1308-120T>G NP_001159906.1:n.1308-120T>G
NM_001166435.2:c.870-120T>G NP_001159907.1:n.870-120T>G
NM_001166436.2:c.870-120T>G NP_001159908.1:n.870-120T>G
NM_002215.3:c.1734-120T>G NP_002206.2:n.1734-120T>G
NM_002215.4:c.1734-120T>G MANE Select NP_002206.2:n.1734-120T>G
NM_001166434.3:c.1308-120T>G NP_001159906.1:n.1308-120T>G