Canonical Allele Identifier: CA1152754104
Gene: SPSB1 HGNC NCBI

Linked Data

dbSNP Id: rs368684339

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348886G>A , CM000663.2:g.9348886G>A GRCh38
NC_000001.10:g.9408945G>A , CM000663.1:g.9408945G>A GRCh37
NC_000001.9:g.9331532G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000328089.11:c.-149-6857G>A MANE Select ENSP00000330221.6:n.-149-6857G>A
ENST00000328089.10:c.-149-6857G>A ENSP00000330221.6:n.-149-6857G>A
ENST00000450402.1:c.-149-6857G>A ENSP00000409235.1:n.-149-6857G>A
NM_025106.3:c.-149-6857G>A NP_079382.2:n.-149-6857G>A
NM_025106.4:c.-149-6857G>A MANE Select NP_079382.2:n.-149-6857G>A