Canonical Allele Identifier: CA2647757801
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149927653-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927653A>C , CM000663.2:g.149927653A>C GRCh38
NC_000001.10:g.149899545A>C , CM000663.1:g.149899545A>C GRCh37
NC_000001.9:g.148166169A>C NCBI36
NG_032777.1:g.5600T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.34+73T>G MANE Select ENSP00000271628.8:n.34+73T>G
ENST00000271628.8:c.34+73T>G ENSP00000271628.8:n.34+73T>G
NM_005850.4:c.34+73T>G NP_005841.1:n.34+73T>G
NM_005850.5:c.34+73T>G MANE Select NP_005841.1:n.34+73T>G
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