Canonical Allele Identifier: CA889161608
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1417878248
gnomAD v4: 1-149926113-A-G
MyVariant Identifiers: chr1:g.149926113A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926113A>G , CM000663.2:g.149926113A>G GRCh38
NC_000001.10:g.149898005A>G , CM000663.1:g.149898005A>G GRCh37
NC_000001.9:g.148164629A>G NCBI36
NG_032777.1:g.7140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.707-71T>C MANE Select ENSP00000271628.8:n.707-71T>C
ENST00000271628.8:c.707-71T>C ENSP00000271628.8:n.707-71T>C
NM_005850.4:c.707-71T>C NP_005841.1:n.707-71T>C
NM_005850.5:c.707-71T>C MANE Select NP_005841.1:n.707-71T>C
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