Canonical Allele Identifier: CA420670479
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1571522912
gnomAD v3: 1-149923641-T-G
gnomAD v4: 1-149923641-T-G
MyVariant Identifiers: chr1:g.149895533T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149923641T>G , CM000663.2:g.149923641T>G GRCh38
NC_000001.10:g.149895533T>G , CM000663.1:g.149895533T>G GRCh37
NC_000001.9:g.148162157T>G NCBI36
NG_032777.1:g.9612A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.1176A>C MANE Select ENSP00000271628.8:p.Pro392=
ENST00000271628.8:c.1176A>C ENSP00000271628.8:p.Pro392=
NM_005850.4:c.1176A>C NP_005841.1:p.Pro392=
NM_005850.5:c.1176A>C MANE Select NP_005841.1:p.Pro392=
Search 100 bp 5'
Search 100 bp 3'