Canonical Allele Identifier: CA671975535

Gene: HTR3B

Linked Data

• dbSNP Id: rs1244436277
• MyVariant Identifiers: chr11:g.113802775A>G (hg19) ; chr11:g.113932053A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932053A>G , CM000673.2:g.113932053A>G	GRCh38
NC_000011.9:g.113802775A>G , CM000673.1:g.113802775A>G	GRCh37
NC_000011.8:g.113307985A>G	NCBI36
NG_011483.1:g.32187A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.368+186A>G MANE Select	ENSP00000260191.2:n.368+186A>G
ENST00000260191.7:c.368+186A>G	ENSP00000260191.2:n.368+186A>G
ENST00000260191.6:c.368+186A>G	ENSP00000260191.2:n.368+186A>G
ENST00000537778.5:c.335+186A>G	ENSP00000443118.1:n.335+186A>G
ENST00000543092.1:c.154+186A>G
NM_006028.4:c.368+186A>G	NP_006019.1:n.368+186A>G
XM_011543063.1:c.335+186A>G	XP_011541365.1:n.335+186A>G
XM_011543064.1:c.167+186A>G	XP_011541366.1:n.167+186A>G
XM_011543065.1:c.161+186A>G	XP_011541367.1:n.161+186A>G
XM_011543066.1:c.335+186A>G	XP_011541368.1:n.335+186A>G
NM_001363563.1:c.335+186A>G	NP_001350492.1:n.335+186A>G
XM_017018552.2:c.161+186A>G	XP_016874041.1:n.161+186A>G
XM_024448767.1:c.74+186A>G	XP_024304535.1:n.74+186A>G
XR_001748034.2:n.619+186A>G
NM_001363563.2:c.335+186A>G	NP_001350492.1:n.335+186A>G
NM_006028.5:c.368+186A>G MANE Select	NP_006019.1:n.368+186A>G