Canonical Allele Identifier: CA2647757084
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149926069-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926069G>T , CM000663.2:g.149926069G>T GRCh38
NC_000001.10:g.149897961G>T , CM000663.1:g.149897961G>T GRCh37
NC_000001.9:g.148164585G>T NCBI36
NG_032777.1:g.7184C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.707-27C>A MANE Select ENSP00000271628.8:n.707-27C>A
ENST00000271628.8:c.707-27C>A ENSP00000271628.8:n.707-27C>A
NM_005850.4:c.707-27C>A NP_005841.1:n.707-27C>A
NM_005850.5:c.707-27C>A MANE Select NP_005841.1:n.707-27C>A
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