Canonical Allele Identifier: CA342275996
Gene: SF3B4 HGNC NCBI

Linked Data

gnomAD v4: 1-149925965-G-T
MyVariant Identifiers: chr1:g.149897857G>T (hg19) chr1:g.149925965G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149925965G>T , CM000663.2:g.149925965G>T GRCh38
NC_000001.10:g.149897857G>T , CM000663.1:g.149897857G>T GRCh37
NC_000001.9:g.148164481G>T NCBI36
NG_032777.1:g.7288C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.784C>A MANE Select ENSP00000271628.8:p.Pro262Thr
ENST00000271628.8:c.784C>A ENSP00000271628.8:p.Pro262Thr
NM_005850.4:c.784C>A NP_005841.1:p.Pro262Thr
NM_005850.5:c.784C>A MANE Select NP_005841.1:p.Pro262Thr
Search 100 bp 5'
Search 100 bp 3'