Canonical Allele Identifier: CA889164023
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1448437403
gnomAD v4: 1-149927797-G-A
MyVariant Identifiers: chr1:g.149927797G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927797G>A , CM000663.2:g.149927797G>A GRCh38
NC_000001.10:g.149899689G>A , CM000663.1:g.149899689G>A GRCh37
NC_000001.9:g.148166313G>A NCBI36
NG_032777.1:g.5456C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.-38C>T MANE Select ENSP00000271628.8:n.-38C>T
ENST00000271628.8:c.-38C>T ENSP00000271628.8:n.-38C>T
NM_005850.4:c.-38C>T NP_005841.1:n.-38C>T
NM_005850.5:c.-38C>T MANE Select NP_005841.1:n.-38C>T
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