Canonical Allele Identifier: CA2216835961

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993143C= , CM000678.2:g.30993143C=	GRCh38
NC_000016.9:g.31004464C= , CM000678.1:g.31004464C=	GRCh37
NC_000016.8:g.30911965C=	NCBI36
NG_041829.1:g.22366G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.773G= MANE Select	ENSP00000215095.5:p.Ser258=
ENST00000565419.2:c.773G=	ENSP00000455899.1:p.Ser258=
ENST00000215095.9:c.773G=	ENSP00000215095.5:p.Ser258=
ENST00000565419.1:c.773G=	ENSP00000455899.1:p.Ser258=
ENST00000569638.5:c.521G=	ENSP00000457067.1:p.Ser174=
NM_052874.4:c.773G=	NP_443106.1:p.Ser258=
XM_017022893.1:c.755G=	XP_016878382.1:p.Ser252=
NM_052874.5:c.773G= MANE Select	NP_443106.1:p.Ser258=