Canonical Allele Identifier: CA342279605

Gene: SF3B4

Linked Data

• dbSNP Id: rs1553766263
• gnomAD v2: 1-149899617-C-T
• gnomAD v4: 1-149927725-C-T
• MyVariant Identifiers: chr1:g.149899617C>T (hg19) ; chr1:g.149927725C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149927725C>T , CM000663.2:g.149927725C>T	GRCh38
NC_000001.10:g.149899617C>T , CM000663.1:g.149899617C>T	GRCh37
NC_000001.9:g.148166241C>T	NCBI36
NG_032777.1:g.5528G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.34+1G>A MANE Select	ENSP00000271628.8:n.34+1G>A
ENST00000271628.8:c.34+1G>A	ENSP00000271628.8:n.34+1G>A
NM_005850.4:c.34+1G>A	NP_005841.1:n.34+1G>A
NM_005850.5:c.34+1G>A MANE Select	NP_005841.1:n.34+1G>A