Canonical Allele Identifier: CA1365040206
Gene: ITIH4 HGNC NCBI

Linked Data

dbSNP Id: rs1578780455

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52825607T>C , CM000665.2:g.52825607T>C GRCh38
NC_000003.11:g.52859623T>C , CM000665.1:g.52859623T>C GRCh37
NC_000003.10:g.52834663T>C NCBI36
NG_016006.1:g.10095A>G
NG_016006.2:g.10095A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000266041.9:c.759+279A>G MANE Select ENSP00000266041.4:n.759+279A>G
ENST00000266041.8:c.759+279A>G ENSP00000266041.4:n.759+279A>G
ENST00000406595.5:c.759+279A>G ENSP00000384425.1:n.759+279A>G
ENST00000441637.2:c.331+279A>G
ENST00000468472.1:c.*891+279A>G ENSP00000422253.1:n.*891+279A>G
ENST00000485816.5:c.759+279A>G ENSP00000417824.1:n.759+279A>G
ENST00000491663.5:n.804+279A>G
ENST00000537897.5:n.644+279A>G
NM_001166449.1:c.759+279A>G NP_001159921.1:n.759+279A>G
NM_002218.4:c.759+279A>G NP_002209.2:n.759+279A>G
NM_002218.5:c.759+279A>G MANE Select NP_002209.2:n.759+279A>G
NM_001166449.2:c.759+279A>G NP_001159921.1:n.759+279A>G