Canonical Allele Identifier: CA280574890

Gene: STX1B

Linked Data

• dbSNP Id: rs899076167
• gnomAD v3: 16-30999768-C-T
• gnomAD v4: 16-30999768-C-T
• MyVariant Identifiers: chr16:g.31011089C>T (hg19) ; chr16:g.30999768C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30999768C>T , CM000678.2:g.30999768C>T	GRCh38
NC_000016.9:g.31011089C>T , CM000678.1:g.31011089C>T	GRCh37
NC_000016.8:g.30918590C>T	NCBI36
NG_041829.1:g.15741G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.280+1160G>A MANE Select	ENSP00000215095.5:n.280+1160G>A
ENST00000565419.2:c.280+1160G>A	ENSP00000455899.1:n.280+1160G>A
ENST00000215095.9:c.280+1160G>A	ENSP00000215095.5:n.280+1160G>A
ENST00000565419.1:c.280+1160G>A	ENSP00000455899.1:n.280+1160G>A
ENST00000569638.5:c.28+1160G>A	ENSP00000457067.1:n.28+1160G>A
NM_052874.4:c.280+1160G>A	NP_443106.1:n.280+1160G>A
XM_017022893.1:c.262+1160G>A	XP_016878382.1:n.262+1160G>A
NM_052874.5:c.280+1160G>A MANE Select	NP_443106.1:n.280+1160G>A