Canonical Allele Identifier: CA420671942
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897864T>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925972T>C , CM000663.2:g.149925972T>C GRCh38
NC_000001.10:g.149897864T>C , CM000663.1:g.149897864T>C GRCh37
NC_000001.9:g.148164488T>C NCBI36
NG_032777.1:g.7281A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.777A>G MANE Select ENSP00000271628.8:p.Pro259=
ENST00000271628.8:c.777A>G ENSP00000271628.8:p.Pro259=
NM_005850.4:c.777A>G NP_005841.1:p.Pro259=
NM_005850.5:c.777A>G MANE Select NP_005841.1:p.Pro259=
Search 100 bp 5'
Search 100 bp 3'