Canonical Allele Identifier: CA29990860
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs495204
MyVariant Identifiers: chr1:g.149898120C>T (hg19) chr1:g.149926228C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926228C>T , CM000663.2:g.149926228C>T GRCh38
NC_000001.10:g.149898120C>T , CM000663.1:g.149898120C>T GRCh37
NC_000001.9:g.148164744C>T NCBI36
NG_032777.1:g.7025G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.706+148G>A MANE Select ENSP00000271628.8:n.706+148G>A
ENST00000271628.8:c.706+148G>A ENSP00000271628.8:n.706+148G>A
NM_005850.4:c.706+148G>A NP_005841.1:n.706+148G>A
NM_005850.5:c.706+148G>A MANE Select NP_005841.1:n.706+148G>A
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