Canonical Allele Identifier: CA280574945

Gene: STX1B

Linked Data

• dbSNP Id: rs764623827
• gnomAD v3: 16-30999911-T-G
• gnomAD v4: 16-30999911-T-G
• MyVariant Identifiers: chr16:g.31011232T>G (hg19) ; chr16:g.30999911T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30999911T>G , CM000678.2:g.30999911T>G	GRCh38
NC_000016.9:g.31011232T>G , CM000678.1:g.31011232T>G	GRCh37
NC_000016.8:g.30918733T>G	NCBI36
NG_041829.1:g.15598A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.280+1017A>C MANE Select	ENSP00000215095.5:n.280+1017A>C
ENST00000565419.2:c.280+1017A>C	ENSP00000455899.1:n.280+1017A>C
ENST00000215095.9:c.280+1017A>C	ENSP00000215095.5:n.280+1017A>C
ENST00000565419.1:c.280+1017A>C	ENSP00000455899.1:n.280+1017A>C
ENST00000569638.5:c.28+1017A>C	ENSP00000457067.1:n.28+1017A>C
NM_052874.4:c.280+1017A>C	NP_443106.1:n.280+1017A>C
XM_017022893.1:c.262+1017A>C	XP_016878382.1:n.262+1017A>C
NM_052874.5:c.280+1017A>C MANE Select	NP_443106.1:n.280+1017A>C