Canonical Allele Identifier: CA2216843658
Gene: STX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30999815A= , CM000678.2:g.30999815A= GRCh38
NC_000016.9:g.31011136A= , CM000678.1:g.31011136A= GRCh37
NC_000016.8:g.30918637A= NCBI36
NG_041829.1:g.15694T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215095.11:c.280+1113T= MANE Select ENSP00000215095.5:n.280+1113T=
ENST00000565419.2:c.280+1113T= ENSP00000455899.1:n.280+1113T=
ENST00000215095.9:c.280+1113T= ENSP00000215095.5:n.280+1113T=
ENST00000565419.1:c.280+1113T= ENSP00000455899.1:n.280+1113T=
ENST00000569638.5:c.28+1113T= ENSP00000457067.1:n.28+1113T=
NM_052874.4:c.280+1113T= NP_443106.1:n.280+1113T=
XM_017022893.1:c.262+1113T= XP_016878382.1:n.262+1113T=
NM_052874.5:c.280+1113T= MANE Select NP_443106.1:n.280+1113T=