Canonical Allele Identifier: CA889163689
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1406566353
gnomAD v4: 1-149927554-C-T
MyVariant Identifiers: chr1:g.149927554C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927554C>T , CM000663.2:g.149927554C>T GRCh38
NC_000001.10:g.149899446C>T , CM000663.1:g.149899446C>T GRCh37
NC_000001.9:g.148166070C>T NCBI36
NG_032777.1:g.5699G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.34+172G>A MANE Select ENSP00000271628.8:n.34+172G>A
ENST00000271628.8:c.34+172G>A ENSP00000271628.8:n.34+172G>A
ENST00000457312.1:c.-218G>A ENSP00000391114.1:n.-218G>A
NM_005850.4:c.34+172G>A NP_005841.1:n.34+172G>A
NM_005850.5:c.34+172G>A MANE Select NP_005841.1:n.34+172G>A
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