Canonical Allele Identifier: CA395646775

Gene: STX1B

Linked Data

• MyVariant Identifiers: chr16:g.31004492C>A (hg19) ; chr16:g.30993171C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993171C>A , CM000678.2:g.30993171C>A	GRCh38
NC_000016.9:g.31004492C>A , CM000678.1:g.31004492C>A	GRCh37
NC_000016.8:g.30911993C>A	NCBI36
NG_041829.1:g.22338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.745G>T MANE Select	ENSP00000215095.5:p.Asp249Tyr
ENST00000565419.2:c.745G>T	ENSP00000455899.1:p.Asp249Tyr
ENST00000215095.9:c.745G>T	ENSP00000215095.5:p.Asp249Tyr
ENST00000565419.1:c.745G>T	ENSP00000455899.1:p.Asp249Tyr
ENST00000569638.5:c.493G>T	ENSP00000457067.1:p.Asp165Tyr
NM_052874.4:c.745G>T	NP_443106.1:p.Asp249Tyr
XM_017022893.1:c.727G>T	XP_016878382.1:p.Asp243Tyr
NM_052874.5:c.745G>T MANE Select	NP_443106.1:p.Asp249Tyr