Canonical Allele Identifier: CA2580575910
Gene: STX1B HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30999862A>T , CM000678.2:g.30999862A>T GRCh38
NC_000016.9:g.31011183A>T , CM000678.1:g.31011183A>T GRCh37
NC_000016.8:g.30918684A>T NCBI36
NG_041829.1:g.15647T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000215095.11:c.280+1066T>A MANE Select ENSP00000215095.5:n.280+1066T>A
ENST00000565419.2:c.280+1066T>A ENSP00000455899.1:n.280+1066T>A
ENST00000215095.9:c.280+1066T>A ENSP00000215095.5:n.280+1066T>A
ENST00000565419.1:c.280+1066T>A ENSP00000455899.1:n.280+1066T>A
ENST00000569638.5:c.28+1066T>A ENSP00000457067.1:n.28+1066T>A
NM_052874.4:c.280+1066T>A NP_443106.1:n.280+1066T>A
XM_017022893.1:c.262+1066T>A XP_016878382.1:n.262+1066T>A
NM_052874.5:c.280+1066T>A MANE Select NP_443106.1:n.280+1066T>A
Search 100 bp 5'
Search 100 bp 3'