Canonical Allele Identifier: CA420672381
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149926380-T-G
MyVariant Identifiers: chr1:g.149898272T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926380T>G , CM000663.2:g.149926380T>G GRCh38
NC_000001.10:g.149898272T>G , CM000663.1:g.149898272T>G GRCh37
NC_000001.9:g.148164896T>G NCBI36
NG_032777.1:g.6873A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.702A>C MANE Select ENSP00000271628.8:p.Pro234=
ENST00000271628.8:c.702A>C ENSP00000271628.8:p.Pro234=
NM_005850.4:c.702A>C NP_005841.1:p.Pro234=
NM_005850.5:c.702A>C MANE Select NP_005841.1:p.Pro234=
Search 100 bp 5'
Search 100 bp 3'