Canonical Allele Identifier: CA29990794
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs587707747
gnomAD v3: 1-149926118-G-A
gnomAD v4: 1-149926118-G-A
MyVariant Identifiers: chr1:g.149898010G>A (hg19) chr1:g.149926118G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926118G>A , CM000663.2:g.149926118G>A GRCh38
NC_000001.10:g.149898010G>A , CM000663.1:g.149898010G>A GRCh37
NC_000001.9:g.148164634G>A NCBI36
NG_032777.1:g.7135C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.707-76C>T MANE Select ENSP00000271628.8:n.707-76C>T
ENST00000271628.8:c.707-76C>T ENSP00000271628.8:n.707-76C>T
NM_005850.4:c.707-76C>T NP_005841.1:n.707-76C>T
NM_005850.5:c.707-76C>T MANE Select NP_005841.1:n.707-76C>T
Search 100 bp 5'
Search 100 bp 3'