Canonical Allele Identifier: CA395646691

Gene: STX1B

Linked Data

• MyVariant Identifiers: chr16:g.31004474T>A (hg19) ; chr16:g.30993153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993153T>A , CM000678.2:g.30993153T>A	GRCh38
NC_000016.9:g.31004474T>A , CM000678.1:g.31004474T>A	GRCh37
NC_000016.8:g.30911975T>A	NCBI36
NG_041829.1:g.22356A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.763A>T MANE Select	ENSP00000215095.5:p.Lys255Ter
ENST00000565419.2:c.763A>T	ENSP00000455899.1:p.Lys255Ter
ENST00000215095.9:c.763A>T	ENSP00000215095.5:p.Lys255Ter
ENST00000565419.1:c.763A>T	ENSP00000455899.1:p.Lys255Ter
ENST00000569638.5:c.511A>T	ENSP00000457067.1:p.Lys171Ter
NM_052874.4:c.763A>T	NP_443106.1:p.Lys255Ter
XM_017022893.1:c.745A>T	XP_016878382.1:p.Lys249Ter
NM_052874.5:c.763A>T MANE Select	NP_443106.1:p.Lys255Ter