Canonical Allele Identifier: CA2647757161

Gene: SF3B4

Linked Data

• gnomAD v4: 1-149926144-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149926144_149926145insT , CM000663.2:g.149926144_149926145insT	GRCh38
NC_000001.10:g.149898036_149898037insT , CM000663.1:g.149898036_149898037insT	GRCh37
NC_000001.9:g.148164660_148164661insT	NCBI36
NG_032777.1:g.7108_7109insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.707-103_707-102insA MANE Select	ENSP00000271628.8:n.707-103_707-102insA
ENST00000271628.8:c.707-103_707-102insA	ENSP00000271628.8:n.707-103_707-102insA
NM_005850.4:c.707-103_707-102insA	NP_005841.1:n.707-103_707-102insA
NM_005850.5:c.707-103_707-102insA MANE Select	NP_005841.1:n.707-103_707-102insA