Canonical Allele Identifier: CA521113445
Gene: SPSB1 HGNC NCBI

Linked Data

dbSNP Id: rs1164896055
gnomAD v2: 1-9408770-A-G
gnomAD v3: 1-9348711-A-G
gnomAD v4: 1-9348711-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348711A>G , CM000663.2:g.9348711A>G GRCh38
NC_000001.10:g.9408770A>G , CM000663.1:g.9408770A>G GRCh37
NC_000001.9:g.9331357A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328089.11:c.-149-7032A>G MANE Select ENSP00000330221.6:n.-149-7032A>G
ENST00000328089.10:c.-149-7032A>G ENSP00000330221.6:n.-149-7032A>G
ENST00000450402.1:c.-149-7032A>G ENSP00000409235.1:n.-149-7032A>G
NM_025106.3:c.-149-7032A>G NP_079382.2:n.-149-7032A>G
NM_025106.4:c.-149-7032A>G MANE Select NP_079382.2:n.-149-7032A>G