Canonical Allele Identifier: CA2632804608

Gene: STX1B

Linked Data

• gnomAD v4: 16-30993292-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993292G>A , CM000678.2:g.30993292G>A	GRCh38
NC_000016.9:g.31004613G>A , CM000678.1:g.31004613G>A	GRCh37
NC_000016.8:g.30912114G>A	NCBI36
NG_041829.1:g.22217C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.676-52C>T MANE Select	ENSP00000215095.5:n.676-52C>T
ENST00000565419.2:c.676-52C>T	ENSP00000455899.1:n.676-52C>T
ENST00000215095.9:c.676-52C>T	ENSP00000215095.5:n.676-52C>T
ENST00000565419.1:c.676-52C>T	ENSP00000455899.1:n.676-52C>T
ENST00000569638.5:c.424-52C>T	ENSP00000457067.1:n.424-52C>T
NM_052874.4:c.676-52C>T	NP_443106.1:n.676-52C>T
XM_017022893.1:c.658-52C>T	XP_016878382.1:n.658-52C>T
NM_052874.5:c.676-52C>T MANE Select	NP_443106.1:n.676-52C>T