Canonical Allele Identifier: CA342276298
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149898290C>A (hg19) chr1:g.149926398C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926398C>A , CM000663.2:g.149926398C>A GRCh38
NC_000001.10:g.149898290C>A , CM000663.1:g.149898290C>A GRCh37
NC_000001.9:g.148164914C>A NCBI36
NG_032777.1:g.6855G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.684G>T MANE Select ENSP00000271628.8:p.Leu228Phe
ENST00000271628.8:c.684G>T ENSP00000271628.8:p.Leu228Phe
ENST00000457312.1:c.555G>T ENSP00000391114.1:p.Leu185Phe
NM_005850.4:c.684G>T NP_005841.1:p.Leu228Phe
NM_005850.5:c.684G>T MANE Select NP_005841.1:p.Leu228Phe
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