Canonical Allele Identifier: CA390037013

Gene: SPTB

Linked Data

• MyVariant Identifiers: chr14:g.65220376T>G (hg19) ; chr14:g.64753658T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.64753658T>G , CM000676.2:g.64753658T>G	GRCh38
NC_000014.8:g.65220376T>G , CM000676.1:g.65220376T>G	GRCh37
NC_000014.7:g.64290129T>G	NCBI36
NG_016202.1:g.74491A>C
NG_016202.2:g.131235A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342835.9:n.218A>C
ENST00000644917.1:c.6481A>C MANE Select	ENSP00000495909.1:p.Ser2161Arg
ENST00000342835.8:n.218A>C
ENST00000389722.7:c.6481A>C	ENSP00000374372.3:p.Ser2161Arg
ENST00000553938.5:c.2476A>C	ENSP00000451324.1:p.Ser826Arg
ENST00000556227.1:n.3884A>C
ENST00000556626.5:c.6481A>C	ENSP00000451752.1:p.Ser2161Arg
NM_001024858.2:c.6481A>C	NP_001020029.1:p.Ser2161Arg
XM_005268023.3:c.6481A>C	XP_005268080.1:p.Ser2161Arg
NM_001024858.3:c.6481A>C	NP_001020029.1:p.Ser2161Arg
NM_001355436.2:c.6481A>C MANE Select	NP_001342365.1:p.Ser2161Arg
XM_017021612.2:c.6481A>C	XP_016877101.1:p.Ser2161Arg
XM_024449699.1:c.6481A>C	XP_024305467.1:p.Ser2161Arg
NM_001024858.4:c.6481A>C	NP_001020029.1:p.Ser2161Arg