Canonical Allele Identifier: CA420672370
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1553766022
gnomAD v2: 1-149898269-T-A
gnomAD v4: 1-149926377-T-A
MyVariant Identifiers: chr1:g.149898269T>A (hg19) chr1:g.149926377T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926377T>A , CM000663.2:g.149926377T>A GRCh38
NC_000001.10:g.149898269T>A , CM000663.1:g.149898269T>A GRCh37
NC_000001.9:g.148164893T>A NCBI36
NG_032777.1:g.6876A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.705A>T MANE Select ENSP00000271628.8:p.Pro235=
ENST00000271628.8:c.705A>T ENSP00000271628.8:p.Pro235=
NM_005850.4:c.705A>T NP_005841.1:p.Pro235=
NM_005850.5:c.705A>T MANE Select NP_005841.1:p.Pro235=
Search 100 bp 5'
Search 100 bp 3'