Canonical Allele Identifier: CA342279682
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149927744-T-C
MyVariant Identifiers: chr1:g.149899636T>C (hg19) chr1:g.149927744T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927744T>C , CM000663.2:g.149927744T>C GRCh38
NC_000001.10:g.149899636T>C , CM000663.1:g.149899636T>C GRCh37
NC_000001.9:g.148166260T>C NCBI36
NG_032777.1:g.5509A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.16A>G MANE Select ENSP00000271628.8:p.Ile6Val
ENST00000271628.8:c.16A>G ENSP00000271628.8:p.Ile6Val
NM_005850.4:c.16A>G NP_005841.1:p.Ile6Val
NM_005850.5:c.16A>G MANE Select NP_005841.1:p.Ile6Val
Search 100 bp 5'
Search 100 bp 3'