Canonical Allele Identifier: CA420672395

Gene: SF3B4

Linked Data

• MyVariant Identifiers: chr1:g.149898275A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149926383A>C , CM000663.2:g.149926383A>C	GRCh38
NC_000001.10:g.149898275A>C , CM000663.1:g.149898275A>C	GRCh37
NC_000001.9:g.148164899A>C	NCBI36
NG_032777.1:g.6870T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.699T>G MANE Select	ENSP00000271628.8:p.Pro233=
ENST00000271628.8:c.699T>G	ENSP00000271628.8:p.Pro233=
ENST00000457312.1:c.570T>G	ENSP00000391114.1:p.Pro190=
NM_005850.4:c.699T>G	NP_005841.1:p.Pro233=
NM_005850.5:c.699T>G MANE Select	NP_005841.1:p.Pro233=