Canonical Allele Identifier: CA395646627
Gene: STX1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30993144T>A , CM000678.2:g.30993144T>A GRCh38
NC_000016.9:g.31004465T>A , CM000678.1:g.31004465T>A GRCh37
NC_000016.8:g.30911966T>A NCBI36
NG_041829.1:g.22365A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215095.11:c.772A>T MANE Select ENSP00000215095.5:p.Ser258Cys
ENST00000565419.2:c.772A>T ENSP00000455899.1:p.Ser258Cys
ENST00000215095.9:c.772A>T ENSP00000215095.5:p.Ser258Cys
ENST00000565419.1:c.772A>T ENSP00000455899.1:p.Ser258Cys
ENST00000569638.5:c.520A>T ENSP00000457067.1:p.Ser174Cys
NM_052874.4:c.772A>T NP_443106.1:p.Ser258Cys
XM_017022893.1:c.754A>T XP_016878382.1:p.Ser252Cys
NM_052874.5:c.772A>T MANE Select NP_443106.1:p.Ser258Cys