Canonical Allele Identifier: CA29990881
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1028115104
gnomAD v2: 1-149898193-T-A
gnomAD v3: 1-149926301-T-A
gnomAD v4: 1-149926301-T-A
MyVariant Identifiers: chr1:g.149898193T>A (hg19) chr1:g.149926301T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149926301T>A , CM000663.2:g.149926301T>A GRCh38
NC_000001.10:g.149898193T>A , CM000663.1:g.149898193T>A GRCh37
NC_000001.9:g.148164817T>A NCBI36
NG_032777.1:g.6952A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000271628.9:c.706+75A>T MANE Select ENSP00000271628.8:n.706+75A>T
ENST00000271628.8:c.706+75A>T ENSP00000271628.8:n.706+75A>T
NM_005850.4:c.706+75A>T NP_005841.1:n.706+75A>T
NM_005850.5:c.706+75A>T MANE Select NP_005841.1:n.706+75A>T
Search 100 bp 5'
Search 100 bp 3'