Canonical Allele Identifier: CA262682837
Gene: SPTB HGNC NCBI

Linked Data

dbSNP Id: rs745476248

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.64767781C>T , CM000676.2:g.64767781C>T GRCh38
NC_000014.8:g.65234499C>T , CM000676.1:g.65234499C>T GRCh37
NC_000014.7:g.64304252C>T NCBI36
NG_016202.1:g.60368G>A
NG_016202.2:g.117112G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389720.4:c.6101G>A ENSP00000374370.4:p.Ser2034Asn
ENST00000644917.1:c.6101G>A MANE Select ENSP00000495909.1:p.Ser2034Asn
ENST00000389720.3:c.6101G>A ENSP00000374370.3:p.Ser2034Asn
ENST00000389721.9:c.6101G>A ENSP00000374371.5:p.Ser2034Asn
ENST00000389722.7:c.6101G>A ENSP00000374372.3:p.Ser2034Asn
ENST00000542694.2:n.433G>A
ENST00000553938.5:c.2096G>A ENSP00000451324.1:p.Ser699Asn
ENST00000556626.5:c.6101G>A ENSP00000451752.1:p.Ser2034Asn
NM_000347.5:c.6101G>A NP_000338.3:p.Ser2034Asn
NM_001024858.2:c.6101G>A NP_001020029.1:p.Ser2034Asn
XM_005268023.3:c.6101G>A XP_005268080.1:p.Ser2034Asn
NM_001024858.3:c.6101G>A NP_001020029.1:p.Ser2034Asn
NM_001355436.2:c.6101G>A MANE Select NP_001342365.1:p.Ser2034Asn
NM_001355437.2:c.6101G>A NP_001342366.1:p.Ser2034Asn
XM_017021612.2:c.6101G>A XP_016877101.1:p.Ser2034Asn
XM_024449699.1:c.6101G>A XP_024305467.1:p.Ser2034Asn
NM_001024858.4:c.6101G>A NP_001020029.1:p.Ser2034Asn