Canonical Allele Identifier: CA2216836084

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993208C= , CM000678.2:g.30993208C=	GRCh38
NC_000016.9:g.31004529C= , CM000678.1:g.31004529C=	GRCh37
NC_000016.8:g.30912030C=	NCBI36
NG_041829.1:g.22301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.708G= MANE Select	ENSP00000215095.5:p.Val236=
ENST00000565419.2:c.708G=	ENSP00000455899.1:p.Val236=
ENST00000215095.9:c.708G=	ENSP00000215095.5:p.Val236=
ENST00000565419.1:c.708G=	ENSP00000455899.1:p.Val236=
ENST00000569638.5:c.456G=	ENSP00000457067.1:p.Val152=
NM_052874.4:c.708G=	NP_443106.1:p.Val236=
XM_017022893.1:c.690G=	XP_016878382.1:p.Val230=
NM_052874.5:c.708G= MANE Select	NP_443106.1:p.Val236=