Canonical Allele Identifier: CA342279791
Gene: SF3B4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.149899651T>G (hg19) chr1:g.149927759T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927759T>G , CM000663.2:g.149927759T>G GRCh38
NC_000001.10:g.149899651T>G , CM000663.1:g.149899651T>G GRCh37
NC_000001.9:g.148166275T>G NCBI36
NG_032777.1:g.5494A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.1A>C MANE Select ENSP00000271628.8:p.Met1Leu
ENST00000271628.8:c.1A>C ENSP00000271628.8:p.Met1Leu
NM_005850.4:c.1A>C NP_005841.1:p.Met1Leu
NM_005850.5:c.1A>C MANE Select NP_005841.1:p.Met1Leu
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Search 100 bp 3'