Canonical Allele Identifier: CA889164433
Gene: SF3B4 HGNC NCBI

Linked Data

dbSNP Id: rs1192550802
MyVariant Identifiers: chr1:g.149927939C>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149927939C>G , CM000663.2:g.149927939C>G GRCh38
NC_000001.10:g.149899831C>G , CM000663.1:g.149899831C>G GRCh37
NC_000001.9:g.148166455C>G NCBI36
NG_032777.1:g.5314G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000271628.8:c.-180G>C ENSP00000271628.8:n.-180G>C
NM_005850.4:c.-180G>C NP_005841.1:n.-180G>C