Canonical Allele Identifier: CA889163945
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1414889507
gnomAD v4: 1-149927766-A-T
MyVariant Identifiers: chr1:g.149927766A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927766A>T , CM000663.2:g.149927766A>T GRCh38
NC_000001.10:g.149899658A>T , CM000663.1:g.149899658A>T GRCh37
NC_000001.9:g.148166282A>T NCBI36
NG_032777.1:g.5487T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.-7T>A MANE Select ENSP00000271628.8:n.-7T>A
ENST00000271628.8:c.-7T>A ENSP00000271628.8:n.-7T>A
NM_005850.4:c.-7T>A NP_005841.1:n.-7T>A
NM_005850.5:c.-7T>A MANE Select NP_005841.1:n.-7T>A
Search 100 bp 5'
Search 100 bp 3'