Canonical Allele Identifier: CA17780216
Gene: SPSB1 HGNC NCBI

Linked Data

dbSNP Id: rs960995221
gnomAD v2: 1-9408935-C-G
gnomAD v3: 1-9348876-C-G
gnomAD v4: 1-9348876-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348876C>G , CM000663.2:g.9348876C>G GRCh38
NC_000001.10:g.9408935C>G , CM000663.1:g.9408935C>G GRCh37
NC_000001.9:g.9331522C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328089.11:c.-149-6867C>G MANE Select ENSP00000330221.6:n.-149-6867C>G
ENST00000328089.10:c.-149-6867C>G ENSP00000330221.6:n.-149-6867C>G
ENST00000450402.1:c.-149-6867C>G ENSP00000409235.1:n.-149-6867C>G
NM_025106.3:c.-149-6867C>G NP_079382.2:n.-149-6867C>G
NM_025106.4:c.-149-6867C>G MANE Select NP_079382.2:n.-149-6867C>G