Canonical Allele Identifier: CA29992078
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs976409008
MyVariant Identifiers: chr1:g.149927849G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927849G>C , CM000663.2:g.149927849G>C GRCh38
NC_000001.10:g.149899741G>C , CM000663.1:g.149899741G>C GRCh37
NC_000001.9:g.148166365G>C NCBI36
NG_032777.1:g.5404C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-90C>G ENSP00000271628.8:n.-90C>G
NM_005850.4:c.-90C>G NP_005841.1:n.-90C>G
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