Canonical Allele Identifier: CA2575973881

Gene: STX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993259T>C , CM000678.2:g.30993259T>C	GRCh38
NC_000016.9:g.31004580T>C , CM000678.1:g.31004580T>C	GRCh37
NC_000016.8:g.30912081T>C	NCBI36
NG_041829.1:g.22250A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.676-19A>G MANE Select	ENSP00000215095.5:n.676-19A>G
ENST00000565419.2:c.676-19A>G	ENSP00000455899.1:n.676-19A>G
ENST00000215095.9:c.676-19A>G	ENSP00000215095.5:n.676-19A>G
ENST00000565419.1:c.676-19A>G	ENSP00000455899.1:n.676-19A>G
ENST00000569638.5:c.424-19A>G	ENSP00000457067.1:n.424-19A>G
NM_052874.4:c.676-19A>G	NP_443106.1:n.676-19A>G
XM_017022893.1:c.658-19A>G	XP_016878382.1:n.658-19A>G
NM_052874.5:c.676-19A>G MANE Select	NP_443106.1:n.676-19A>G