Canonical Allele Identifier: CA526030090
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1453439260
gnomAD v2: 1-149900234-C-T
gnomAD v3: 1-149928342-C-T
gnomAD v4: 1-149928342-C-T
MyVariant Identifiers: chr1:g.149900234C>T (hg19) chr1:g.149928342C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149928342C>T , CM000663.2:g.149928342C>T GRCh38
NC_000001.10:g.149900234C>T , CM000663.1:g.149900234C>T GRCh37
NC_000001.9:g.148166858C>T NCBI36
NG_032777.1:g.4911G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.8:c.-583G>A ENSP00000271628.8:n.-583G>A
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