Canonical Allele Identifier: CA342274880

Gene: SF3B4

Linked Data

• MyVariant Identifiers: chr1:g.149897765A>C (hg19) ; chr1:g.149925873A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149925873A>C , CM000663.2:g.149925873A>C	GRCh38
NC_000001.10:g.149897765A>C , CM000663.1:g.149897765A>C	GRCh37
NC_000001.9:g.148164389A>C	NCBI36
NG_032777.1:g.7380T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271628.9:c.876T>G MANE Select	ENSP00000271628.8:p.His292Gln
ENST00000271628.8:c.876T>G	ENSP00000271628.8:p.His292Gln
NM_005850.4:c.876T>G	NP_005841.1:p.His292Gln
NM_005850.5:c.876T>G MANE Select	NP_005841.1:p.His292Gln