Canonical Allele Identifier: CA2647757703
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149927564-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927564A>G , CM000663.2:g.149927564A>G GRCh38
NC_000001.10:g.149899456A>G , CM000663.1:g.149899456A>G GRCh37
NC_000001.9:g.148166080A>G NCBI36
NG_032777.1:g.5689T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.34+162T>C MANE Select ENSP00000271628.8:n.34+162T>C
ENST00000271628.8:c.34+162T>C ENSP00000271628.8:n.34+162T>C
ENST00000457312.1:c.-228T>C ENSP00000391114.1:n.-228T>C
NM_005850.4:c.34+162T>C NP_005841.1:n.34+162T>C
NM_005850.5:c.34+162T>C MANE Select NP_005841.1:n.34+162T>C
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