Canonical Allele Identifier: CA526030065

Gene: SF3B4

Linked Data

• dbSNP Id: rs1553766353
• gnomAD v2: 1-149899958-G-C
• gnomAD v3: 1-149928066-G-C
• gnomAD v4: 1-149928066-G-C
• MyVariant Identifiers: chr1:g.149899958G>C (hg19) ; chr1:g.149928066G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149928066G>C , CM000663.2:g.149928066G>C	GRCh38
NC_000001.10:g.149899958G>C , CM000663.1:g.149899958G>C	GRCh37
NC_000001.9:g.148166582G>C	NCBI36
NG_032777.1:g.5187C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.8:c.-307C>G	ENSP00000271628.8:n.-307C>G
NM_005850.4:c.-307C>G	NP_005841.1:n.-307C>G