Canonical Allele Identifier: CA395646865

Gene: STX1B

Linked Data

• ClinVar Variation Id: 451862
• ClinVar RCV Id: RCV000519620
• dbSNP Id: rs1555493906
• MyVariant Identifiers: chr16:g.31004522A>G (hg19) ; chr16:g.30993201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993201A>G , CM000678.2:g.30993201A>G	GRCh38
NC_000016.9:g.31004522A>G , CM000678.1:g.31004522A>G	GRCh37
NC_000016.8:g.30912023A>G	NCBI36
NG_041829.1:g.22308T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.715T>C MANE Select	ENSP00000215095.5:p.Ser239Pro
ENST00000565419.2:c.715T>C	ENSP00000455899.1:p.Ser239Pro
ENST00000215095.9:c.715T>C	ENSP00000215095.5:p.Ser239Pro
ENST00000565419.1:c.715T>C	ENSP00000455899.1:p.Ser239Pro
ENST00000569638.5:c.463T>C	ENSP00000457067.1:p.Ser155Pro
NM_052874.4:c.715T>C	NP_443106.1:p.Ser239Pro
XM_017022893.1:c.697T>C	XP_016878382.1:p.Ser233Pro
NM_052874.5:c.715T>C MANE Select	NP_443106.1:p.Ser239Pro