Canonical Allele Identifier: CA395646762

Gene: STX1B

Linked Data

• MyVariant Identifiers: chr16:g.31004488G>C (hg19) ; chr16:g.30993167G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993167G>C , CM000678.2:g.30993167G>C	GRCh38
NC_000016.9:g.31004488G>C , CM000678.1:g.31004488G>C	GRCh37
NC_000016.8:g.30911989G>C	NCBI36
NG_041829.1:g.22342C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.749C>G MANE Select	ENSP00000215095.5:p.Thr250Ser
ENST00000565419.2:c.749C>G	ENSP00000455899.1:p.Thr250Ser
ENST00000215095.9:c.749C>G	ENSP00000215095.5:p.Thr250Ser
ENST00000565419.1:c.749C>G	ENSP00000455899.1:p.Thr250Ser
ENST00000569638.5:c.497C>G	ENSP00000457067.1:p.Thr166Ser
NM_052874.4:c.749C>G	NP_443106.1:p.Thr250Ser
XM_017022893.1:c.731C>G	XP_016878382.1:p.Thr244Ser
NM_052874.5:c.749C>G MANE Select	NP_443106.1:p.Thr250Ser