Canonical Allele Identifier: CA889164761
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1289248193
gnomAD v3: 1-149928227-C-G
gnomAD v4: 1-149928227-C-G
MyVariant Identifiers: chr1:g.149928227C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928227C>G , CM000663.2:g.149928227C>G GRCh38
NC_000001.10:g.149900119C>G , CM000663.1:g.149900119C>G GRCh37
NC_000001.9:g.148166743C>G NCBI36
NG_032777.1:g.5026G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-468G>C ENSP00000271628.8:n.-468G>C
NM_005850.4:c.-468G>C NP_005841.1:n.-468G>C
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