Canonical Allele Identifier: CA740442502
Gene: SPSB1 HGNC NCBI

Linked Data

dbSNP Id: rs1169482953
MyVariant Identifiers: chr1:g.9408916C>T (hg19) chr1:g.9348857C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.9348857C>T , CM000663.2:g.9348857C>T GRCh38
NC_000001.10:g.9408916C>T , CM000663.1:g.9408916C>T GRCh37
NC_000001.9:g.9331503C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000328089.11:c.-149-6886C>T MANE Select ENSP00000330221.6:n.-149-6886C>T
ENST00000328089.10:c.-149-6886C>T ENSP00000330221.6:n.-149-6886C>T
ENST00000450402.1:c.-149-6886C>T ENSP00000409235.1:n.-149-6886C>T
NM_025106.3:c.-149-6886C>T NP_079382.2:n.-149-6886C>T
NM_025106.4:c.-149-6886C>T MANE Select NP_079382.2:n.-149-6886C>T
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