Canonical Allele Identifier: CA420674029
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149899637C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927745C>G , CM000663.2:g.149927745C>G GRCh38
NC_000001.10:g.149899637C>G , CM000663.1:g.149899637C>G GRCh37
NC_000001.9:g.148166261C>G NCBI36
NG_032777.1:g.5508G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.15G>C MANE Select ENSP00000271628.8:p.Pro5=
ENST00000271628.8:c.15G>C ENSP00000271628.8:p.Pro5=
NM_005850.4:c.15G>C NP_005841.1:p.Pro5=
NM_005850.5:c.15G>C MANE Select NP_005841.1:p.Pro5=
Search 100 bp 5'
Search 100 bp 3'