Canonical Allele Identifier: CA420671639
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897789T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925897T>A , CM000663.2:g.149925897T>A GRCh38
NC_000001.10:g.149897789T>A , CM000663.1:g.149897789T>A GRCh37
NC_000001.9:g.148164413T>A NCBI36
NG_032777.1:g.7356A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.852A>T MANE Select ENSP00000271628.8:p.Gly284=
ENST00000271628.8:c.852A>T ENSP00000271628.8:p.Gly284=
NM_005850.4:c.852A>T NP_005841.1:p.Gly284=
NM_005850.5:c.852A>T MANE Select NP_005841.1:p.Gly284=
Search 100 bp 5'
Search 100 bp 3'