Canonical Allele Identifier: CA2216836182
Gene: STX1B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30993252G= , CM000678.2:g.30993252G= GRCh38
NC_000016.9:g.31004573G= , CM000678.1:g.31004573G= GRCh37
NC_000016.8:g.30912074G= NCBI36
NG_041829.1:g.22257C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215095.11:c.676-12C= MANE Select ENSP00000215095.5:n.676-12C=
ENST00000565419.2:c.676-12C= ENSP00000455899.1:n.676-12C=
ENST00000215095.9:c.676-12C= ENSP00000215095.5:n.676-12C=
ENST00000565419.1:c.676-12C= ENSP00000455899.1:n.676-12C=
ENST00000569638.5:c.424-12C= ENSP00000457067.1:n.424-12C=
NM_052874.4:c.676-12C= NP_443106.1:n.676-12C=
XM_017022893.1:c.658-12C= XP_016878382.1:n.658-12C=
NM_052874.5:c.676-12C= MANE Select NP_443106.1:n.676-12C=
Search 100 bp 5'
Search 100 bp 3'