Canonical Allele Identifier: CA420674051
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs2092600465
MyVariant Identifiers: chr1:g.149899646A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927754A>C , CM000663.2:g.149927754A>C GRCh38
NC_000001.10:g.149899646A>C , CM000663.1:g.149899646A>C GRCh37
NC_000001.9:g.148166270A>C NCBI36
NG_032777.1:g.5499T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.6T>G MANE Select ENSP00000271628.8:p.Ala2=
ENST00000271628.8:c.6T>G ENSP00000271628.8:p.Ala2=
NM_005850.4:c.6T>G NP_005841.1:p.Ala2=
NM_005850.5:c.6T>G MANE Select NP_005841.1:p.Ala2=
Search 100 bp 5'
Search 100 bp 3'