Canonical Allele Identifier: CA395646855

Gene: STX1B

Linked Data

• MyVariant Identifiers: chr16:g.31004518A>G (hg19) ; chr16:g.30993197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.30993197A>G , CM000678.2:g.30993197A>G	GRCh38
NC_000016.9:g.31004518A>G , CM000678.1:g.31004518A>G	GRCh37
NC_000016.8:g.30912019A>G	NCBI36
NG_041829.1:g.22312T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215095.11:c.719T>C MANE Select	ENSP00000215095.5:p.Val240Ala
ENST00000565419.2:c.719T>C	ENSP00000455899.1:p.Val240Ala
ENST00000215095.9:c.719T>C	ENSP00000215095.5:p.Val240Ala
ENST00000565419.1:c.719T>C	ENSP00000455899.1:p.Val240Ala
ENST00000569638.5:c.467T>C	ENSP00000457067.1:p.Val156Ala
NM_052874.4:c.719T>C	NP_443106.1:p.Val240Ala
XM_017022893.1:c.701T>C	XP_016878382.1:p.Val234Ala
NM_052874.5:c.719T>C MANE Select	NP_443106.1:p.Val240Ala