Canonical Allele Identifier: CA420672411

Gene: SF3B4

Linked Data

• MyVariant Identifiers: chr1:g.149898278A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149926386A>T , CM000663.2:g.149926386A>T	GRCh38
NC_000001.10:g.149898278A>T , CM000663.1:g.149898278A>T	GRCh37
NC_000001.9:g.148164902A>T	NCBI36
NG_032777.1:g.6867T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.696T>A MANE Select	ENSP00000271628.8:p.Leu232=
ENST00000271628.8:c.696T>A	ENSP00000271628.8:p.Leu232=
ENST00000457312.1:c.567T>A	ENSP00000391114.1:p.Leu189=
NM_005850.4:c.696T>A	NP_005841.1:p.Leu232=
NM_005850.5:c.696T>A MANE Select	NP_005841.1:p.Leu232=