Canonical Allele Identifier: CA342276289
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149898286A>C (hg19) chr1:g.149926394A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926394A>C , CM000663.2:g.149926394A>C GRCh38
NC_000001.10:g.149898286A>C , CM000663.1:g.149898286A>C GRCh37
NC_000001.9:g.148164910A>C NCBI36
NG_032777.1:g.6859T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.688T>G MANE Select ENSP00000271628.8:p.Ser230Ala
ENST00000271628.8:c.688T>G ENSP00000271628.8:p.Ser230Ala
ENST00000457312.1:c.559T>G ENSP00000391114.1:p.Ser187Ala
NM_005850.4:c.688T>G NP_005841.1:p.Ser230Ala
NM_005850.5:c.688T>G MANE Select NP_005841.1:p.Ser230Ala
Search 100 bp 5'
Search 100 bp 3'