Canonical Allele Identifier: CA420671460
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149897741C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925849C>A , CM000663.2:g.149925849C>A GRCh38
NC_000001.10:g.149897741C>A , CM000663.1:g.149897741C>A GRCh37
NC_000001.9:g.148164365C>A NCBI36
NG_032777.1:g.7404G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.9:c.900G>T MANE Select ENSP00000271628.8:p.Gly300=
ENST00000271628.8:c.900G>T ENSP00000271628.8:p.Gly300=
NM_005850.4:c.900G>T NP_005841.1:p.Gly300=
NM_005850.5:c.900G>T MANE Select NP_005841.1:p.Gly300=
Search 100 bp 5'
Search 100 bp 3'