Canonical Allele Identifier: CA420671891
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092587465
MyVariant Identifiers: chr1:g.149897855G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925963G>C , CM000663.2:g.149925963G>C GRCh38
NC_000001.10:g.149897855G>C , CM000663.1:g.149897855G>C GRCh37
NC_000001.9:g.148164479G>C NCBI36
NG_032777.1:g.7290C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.786C>G MANE Select ENSP00000271628.8:p.Pro262=
ENST00000271628.8:c.786C>G ENSP00000271628.8:p.Pro262=
NM_005850.4:c.786C>G NP_005841.1:p.Pro262=
NM_005850.5:c.786C>G MANE Select NP_005841.1:p.Pro262=
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