Canonical Allele Identifier: CA1007561092
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092601795
gnomAD v3: 1-149927859-C-CGTAG
gnomAD v4: 1-149927859-C-CGTAG
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927859_149927860insGTAG , CM000663.2:g.149927859_149927860insGTAG GRCh38
NC_000001.10:g.149899751_149899752insGTAG , CM000663.1:g.149899751_149899752insGTAG GRCh37
NC_000001.9:g.148166375_148166376insGTAG NCBI36
NG_032777.1:g.5393_5394insCTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-101_-100insCTAC ENSP00000271628.8:n.-101_-100insCTAC
NM_005850.4:c.-101_-100insCTAC NP_005841.1:n.-101_-100insCTAC
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