Canonical Allele Identifier: CA526030058

Gene: SF3B4

Linked Data

• dbSNP Id: rs1483338388
• gnomAD v2: 1-149899877-A-C
• gnomAD v3: 1-149927985-A-C
• gnomAD v4: 1-149927985-A-C
• MyVariant Identifiers: chr1:g.149899877A>C (hg19) ; chr1:g.149927985A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149927985A>C , CM000663.2:g.149927985A>C	GRCh38
NC_000001.10:g.149899877A>C , CM000663.1:g.149899877A>C	GRCh37
NC_000001.9:g.148166501A>C	NCBI36
NG_032777.1:g.5268T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.8:c.-226T>G	ENSP00000271628.8:n.-226T>G
NM_005850.4:c.-226T>G	NP_005841.1:n.-226T>G