Canonical Allele Identifier: CA494920831

Gene: STX1B

Linked Data

• MyVariant Identifiers: chr16:g.31004493A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993172A>G , CM000678.2:g.30993172A>G	GRCh38
NC_000016.9:g.31004493A>G , CM000678.1:g.31004493A>G	GRCh37
NC_000016.8:g.30911994A>G	NCBI36
NG_041829.1:g.22337T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.744T>C MANE Select	ENSP00000215095.5:p.Ser248=
ENST00000565419.2:c.744T>C	ENSP00000455899.1:p.Ser248=
ENST00000215095.9:c.744T>C	ENSP00000215095.5:p.Ser248=
ENST00000565419.1:c.744T>C	ENSP00000455899.1:p.Ser248=
ENST00000569638.5:c.492T>C	ENSP00000457067.1:p.Ser164=
NM_052874.4:c.744T>C	NP_443106.1:p.Ser248=
XM_017022893.1:c.726T>C	XP_016878382.1:p.Ser242=
NM_052874.5:c.744T>C MANE Select	NP_443106.1:p.Ser248=