Canonical Allele Identifier: CA2478942266
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092589643
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926278A>C , CM000663.2:g.149926278A>C GRCh38
NC_000001.10:g.149898170A>C , CM000663.1:g.149898170A>C GRCh37
NC_000001.9:g.148164794A>C NCBI36
NG_032777.1:g.6975T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.706+98T>G MANE Select ENSP00000271628.8:n.706+98T>G
ENST00000271628.8:c.706+98T>G ENSP00000271628.8:n.706+98T>G
NM_005850.4:c.706+98T>G NP_005841.1:n.706+98T>G
NM_005850.5:c.706+98T>G MANE Select NP_005841.1:n.706+98T>G
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