Canonical Allele Identifier: CA526029684
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1559798375
gnomAD v2: 1-149897676-C-CA
gnomAD v4: 1-149925784-C-CA
MyVariant Identifiers: chr1:g.149897676_149897677insA (hg19) chr1:g.149925784_149925785insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925785dup , CM000663.2:g.149925785dup GRCh38
NC_000001.10:g.149897677dup , CM000663.1:g.149897677dup GRCh37
NC_000001.9:g.148164301dup NCBI36
NG_032777.1:g.7468dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.913+51dup MANE Select ENSP00000271628.8:n.913+51dup
ENST00000271628.8:c.913+51dup ENSP00000271628.8:n.913+51dup
NM_005850.4:c.913+51dup NP_005841.1:n.913+51dup
NM_005850.5:c.913+51dup MANE Select NP_005841.1:n.913+51dup
Search 100 bp 5'
Search 100 bp 3'