Canonical Allele Identifier: CA526030070
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1266538157
gnomAD v2: 1-149900017-C-A
gnomAD v3: 1-149928125-C-A
gnomAD v4: 1-149928125-C-A
MyVariant Identifiers: chr1:g.149900017C>A (hg19) chr1:g.149928125C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928125C>A , CM000663.2:g.149928125C>A GRCh38
NC_000001.10:g.149900017C>A , CM000663.1:g.149900017C>A GRCh37
NC_000001.9:g.148166641C>A NCBI36
NG_032777.1:g.5128G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-366G>T ENSP00000271628.8:n.-366G>T
NM_005850.4:c.-366G>T NP_005841.1:n.-366G>T
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