Canonical Allele Identifier: CA2216836229

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993308G= , CM000678.2:g.30993308G=	GRCh38
NC_000016.9:g.31004629G= , CM000678.1:g.31004629G=	GRCh37
NC_000016.8:g.30912130G=	NCBI36
NG_041829.1:g.22201C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.675+39C= MANE Select	ENSP00000215095.5:n.675+39C=
ENST00000565419.2:c.675+39C=	ENSP00000455899.1:n.675+39C=
ENST00000215095.9:c.675+39C=	ENSP00000215095.5:n.675+39C=
ENST00000565419.1:c.675+39C=	ENSP00000455899.1:n.675+39C=
ENST00000569638.5:c.423+39C=	ENSP00000457067.1:n.423+39C=
NM_052874.4:c.675+39C=	NP_443106.1:n.675+39C=
XM_017022893.1:c.657+39C=	XP_016878382.1:n.657+39C=
NM_052874.5:c.675+39C= MANE Select	NP_443106.1:n.675+39C=