Canonical Allele Identifier: CA382668984

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803111T>G (hg19) ; chr11:g.113932389T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932389T>G , CM000673.2:g.113932389T>G	GRCh38
NC_000011.9:g.113803111T>G , CM000673.1:g.113803111T>G	GRCh37
NC_000011.8:g.113308321T>G	NCBI36
NG_011483.1:g.32523T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.469T>G MANE Select	ENSP00000260191.2:p.Leu157Val
ENST00000260191.7:c.469T>G	ENSP00000260191.2:p.Leu157Val
ENST00000260191.6:c.469T>G	ENSP00000260191.2:p.Leu157Val
ENST00000537778.5:c.436T>G	ENSP00000443118.1:p.Leu146Val
ENST00000543092.1:c.255T>G
NM_006028.4:c.469T>G	NP_006019.1:p.Leu157Val
XM_011543063.1:c.436T>G	XP_011541365.1:p.Leu146Val
XM_011543064.1:c.268T>G	XP_011541366.1:p.Leu90Val
XM_011543065.1:c.262T>G	XP_011541367.1:p.Leu88Val
XM_011543066.1:c.436T>G	XP_011541368.1:p.Leu146Val
NM_001363563.1:c.436T>G	NP_001350492.1:p.Leu146Val
XM_017018552.2:c.262T>G	XP_016874041.1:p.Leu88Val
XM_024448767.1:c.175T>G	XP_024304535.1:p.Leu59Val
XR_001748034.2:n.720T>G
NM_001363563.2:c.436T>G	NP_001350492.1:p.Leu146Val
NM_006028.5:c.469T>G MANE Select	NP_006019.1:p.Leu157Val