Canonical Allele Identifier: CA2216836179
Gene: STX1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30993251A= , CM000678.2:g.30993251A= GRCh38
NC_000016.9:g.31004572A= , CM000678.1:g.31004572A= GRCh37
NC_000016.8:g.30912073A= NCBI36
NG_041829.1:g.22258T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215095.11:c.676-11T= MANE Select ENSP00000215095.5:n.676-11T=
ENST00000565419.2:c.676-11T= ENSP00000455899.1:n.676-11T=
ENST00000215095.9:c.676-11T= ENSP00000215095.5:n.676-11T=
ENST00000565419.1:c.676-11T= ENSP00000455899.1:n.676-11T=
ENST00000569638.5:c.424-11T= ENSP00000457067.1:n.424-11T=
NM_052874.4:c.676-11T= NP_443106.1:n.676-11T=
XM_017022893.1:c.658-11T= XP_016878382.1:n.658-11T=
NM_052874.5:c.676-11T= MANE Select NP_443106.1:n.676-11T=
Search 100 bp 5'
Search 100 bp 3'