Canonical Allele Identifier: CA342274796
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897727C>A (hg19) chr1:g.149925835C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925835C>A , CM000663.2:g.149925835C>A GRCh38
NC_000001.10:g.149897727C>A , CM000663.1:g.149897727C>A GRCh37
NC_000001.9:g.148164351C>A NCBI36
NG_032777.1:g.7418G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.913+1G>T MANE Select ENSP00000271628.8:n.913+1G>T
ENST00000271628.8:c.913+1G>T ENSP00000271628.8:n.913+1G>T
NM_005850.4:c.913+1G>T NP_005841.1:n.913+1G>T
NM_005850.5:c.913+1G>T MANE Select NP_005841.1:n.913+1G>T
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