Canonical Allele Identifier: CA29992491
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs587606826
gnomAD v2: 1-149899991-A-G
gnomAD v3: 1-149928099-A-G
gnomAD v4: 1-149928099-A-G
MyVariant Identifiers: chr1:g.149899991A>G (hg19) chr1:g.149928099A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928099A>G , CM000663.2:g.149928099A>G GRCh38
NC_000001.10:g.149899991A>G , CM000663.1:g.149899991A>G GRCh37
NC_000001.9:g.148166615A>G NCBI36
NG_032777.1:g.5154T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-340T>C ENSP00000271628.8:n.-340T>C
NM_005850.4:c.-340T>C NP_005841.1:n.-340T>C
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