Canonical Allele Identifier: CA10586708
Gene: SF3B4 HGNC NCBI

Linked Data

ClinVar Variation Id: 259886
ClinVar RCV Id: RCV000241890
dbSNP Id: rs886038566
MyVariant Identifiers: chr1:g.149898578A>G (hg19) chr1:g.149926686A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926686A>G , CM000663.2:g.149926686A>G GRCh38
NC_000001.10:g.149898578A>G , CM000663.1:g.149898578A>G GRCh37
NC_000001.9:g.148165202A>G NCBI36
NG_032777.1:g.6567T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.396T>C MANE Select ENSP00000271628.8:p.Ile132=
ENST00000271628.8:c.396T>C ENSP00000271628.8:p.Ile132=
ENST00000457312.1:c.267T>C ENSP00000391114.1:p.Ile89=
NM_005850.4:c.396T>C NP_005841.1:p.Ile132=
NM_005850.5:c.396T>C MANE Select NP_005841.1:p.Ile132=
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