Canonical Allele Identifier: CA342274872
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897761G>A (hg19) chr1:g.149925869G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925869G>A , CM000663.2:g.149925869G>A GRCh38
NC_000001.10:g.149897761G>A , CM000663.1:g.149897761G>A GRCh37
NC_000001.9:g.148164385G>A NCBI36
NG_032777.1:g.7384C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.880C>T MANE Select ENSP00000271628.8:p.His294Tyr
ENST00000271628.8:c.880C>T ENSP00000271628.8:p.His294Tyr
NM_005850.4:c.880C>T NP_005841.1:p.His294Tyr
NM_005850.5:c.880C>T MANE Select NP_005841.1:p.His294Tyr
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