Canonical Allele Identifier: CA420671738
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149925930-A-G
MyVariant Identifiers: chr1:g.149897822A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925930A>G , CM000663.2:g.149925930A>G GRCh38
NC_000001.10:g.149897822A>G , CM000663.1:g.149897822A>G GRCh37
NC_000001.9:g.148164446A>G NCBI36
NG_032777.1:g.7323T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.819T>C MANE Select ENSP00000271628.8:p.His273=
ENST00000271628.8:c.819T>C ENSP00000271628.8:p.His273=
NM_005850.4:c.819T>C NP_005841.1:p.His273=
NM_005850.5:c.819T>C MANE Select NP_005841.1:p.His273=
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