Canonical Allele Identifier: CA2216843639

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30999785C= , CM000678.2:g.30999785C=	GRCh38
NC_000016.9:g.31011106C= , CM000678.1:g.31011106C=	GRCh37
NC_000016.8:g.30918607C=	NCBI36
NG_041829.1:g.15724G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000215095.11:c.280+1143G= MANE Select	ENSP00000215095.5:n.280+1143G=
ENST00000565419.2:c.280+1143G=	ENSP00000455899.1:n.280+1143G=
ENST00000215095.9:c.280+1143G=	ENSP00000215095.5:n.280+1143G=
ENST00000565419.1:c.280+1143G=	ENSP00000455899.1:n.280+1143G=
ENST00000569638.5:c.28+1143G=	ENSP00000457067.1:n.28+1143G=
NM_052874.4:c.280+1143G=	NP_443106.1:n.280+1143G=
XM_017022893.1:c.262+1143G=	XP_016878382.1:n.262+1143G=
NM_052874.5:c.280+1143G= MANE Select	NP_443106.1:n.280+1143G=