Canonical Allele Identifier: CA420671813
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897840A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925948A>G , CM000663.2:g.149925948A>G GRCh38
NC_000001.10:g.149897840A>G , CM000663.1:g.149897840A>G GRCh37
NC_000001.9:g.148164464A>G NCBI36
NG_032777.1:g.7305T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.801T>C MANE Select ENSP00000271628.8:p.Pro267=
ENST00000271628.8:c.801T>C ENSP00000271628.8:p.Pro267=
NM_005850.4:c.801T>C NP_005841.1:p.Pro267=
NM_005850.5:c.801T>C MANE Select NP_005841.1:p.Pro267=
Search 100 bp 5'
Search 100 bp 3'