Canonical Allele Identifier: CA1071605
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs199754113
ExAC: 1:149899676 C / T
gnomAD v2: 1-149899676-C-T
gnomAD v3: 1-149927784-C-T
gnomAD v4: 1-149927784-C-T
MyVariant Identifiers: chr1:g.149899676C>T (hg19) chr1:g.149927784C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927784C>T , CM000663.2:g.149927784C>T GRCh38
NC_000001.10:g.149899676C>T , CM000663.1:g.149899676C>T GRCh37
NC_000001.9:g.148166300C>T NCBI36
NG_032777.1:g.5469G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.-25G>A MANE Select ENSP00000271628.8:n.-25G>A
ENST00000271628.8:c.-25G>A ENSP00000271628.8:n.-25G>A
NM_005850.4:c.-25G>A NP_005841.1:n.-25G>A
NM_005850.5:c.-25G>A MANE Select NP_005841.1:n.-25G>A
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