Canonical Allele Identifier: CA889163718
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1252580008
gnomAD v3: 1-149927598-G-A
gnomAD v4: 1-149927598-G-A
MyVariant Identifiers: chr1:g.149927598G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927598G>A , CM000663.2:g.149927598G>A GRCh38
NC_000001.10:g.149899490G>A , CM000663.1:g.149899490G>A GRCh37
NC_000001.9:g.148166114G>A NCBI36
NG_032777.1:g.5655C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.34+128C>T MANE Select ENSP00000271628.8:n.34+128C>T
ENST00000271628.8:c.34+128C>T ENSP00000271628.8:n.34+128C>T
NM_005850.4:c.34+128C>T NP_005841.1:n.34+128C>T
NM_005850.5:c.34+128C>T MANE Select NP_005841.1:n.34+128C>T
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