Canonical Allele Identifier: CA2216836139

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993225G= , CM000678.2:g.30993225G=	GRCh38
NC_000016.9:g.31004546G= , CM000678.1:g.31004546G=	GRCh37
NC_000016.8:g.30912047G=	NCBI36
NG_041829.1:g.22284C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.691C= MANE Select	ENSP00000215095.5:p.Arg231=
ENST00000565419.2:c.691C=	ENSP00000455899.1:p.Arg231=
ENST00000215095.9:c.691C=	ENSP00000215095.5:p.Arg231=
ENST00000565419.1:c.691C=	ENSP00000455899.1:p.Arg231=
ENST00000569638.5:c.439C=	ENSP00000457067.1:p.Arg147=
NM_052874.4:c.691C=	NP_443106.1:p.Arg231=
XM_017022893.1:c.673C=	XP_016878382.1:p.Arg225=
NM_052874.5:c.691C= MANE Select	NP_443106.1:p.Arg231=