Canonical Allele Identifier: CA2216843648

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30999798A= , CM000678.2:g.30999798A=	GRCh38
NC_000016.9:g.31011119A= , CM000678.1:g.31011119A=	GRCh37
NC_000016.8:g.30918620A=	NCBI36
NG_041829.1:g.15711T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000215095.11:c.280+1130T= MANE Select	ENSP00000215095.5:n.280+1130T=
ENST00000565419.2:c.280+1130T=	ENSP00000455899.1:n.280+1130T=
ENST00000215095.9:c.280+1130T=	ENSP00000215095.5:n.280+1130T=
ENST00000565419.1:c.280+1130T=	ENSP00000455899.1:n.280+1130T=
ENST00000569638.5:c.28+1130T=	ENSP00000457067.1:n.28+1130T=
NM_052874.4:c.280+1130T=	NP_443106.1:n.280+1130T=
XM_017022893.1:c.262+1130T=	XP_016878382.1:n.262+1130T=
NM_052874.5:c.280+1130T= MANE Select	NP_443106.1:n.280+1130T=