Canonical Allele Identifier: CA420672432
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149926395-C-A
MyVariant Identifiers: chr1:g.149898287C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926395C>A , CM000663.2:g.149926395C>A GRCh38
NC_000001.10:g.149898287C>A , CM000663.1:g.149898287C>A GRCh37
NC_000001.9:g.148164911C>A NCBI36
NG_032777.1:g.6858G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.687G>T MANE Select ENSP00000271628.8:p.Gly229=
ENST00000271628.8:c.687G>T ENSP00000271628.8:p.Gly229=
ENST00000457312.1:c.558G>T ENSP00000391114.1:p.Gly186=
NM_005850.4:c.687G>T NP_005841.1:p.Gly229=
NM_005850.5:c.687G>T MANE Select NP_005841.1:p.Gly229=
Search 100 bp 5'
Search 100 bp 3'