Canonical Allele Identifier: CA382668981

Gene: HTR3B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.469T>A MANE Select	ENSP00000260191.2:p.Leu157Ile
ENST00000260191.7:c.469T>A	ENSP00000260191.2:p.Leu157Ile
ENST00000260191.6:c.469T>A	ENSP00000260191.2:p.Leu157Ile
ENST00000537778.5:c.436T>A	ENSP00000443118.1:p.Leu146Ile
ENST00000543092.1:c.255T>A
NM_006028.4:c.469T>A	NP_006019.1:p.Leu157Ile
XM_011543063.1:c.436T>A	XP_011541365.1:p.Leu146Ile
XM_011543064.1:c.268T>A	XP_011541366.1:p.Leu90Ile
XM_011543065.1:c.262T>A	XP_011541367.1:p.Leu88Ile
XM_011543066.1:c.436T>A	XP_011541368.1:p.Leu146Ile
NM_001363563.1:c.436T>A	NP_001350492.1:p.Leu146Ile
XM_017018552.2:c.262T>A	XP_016874041.1:p.Leu88Ile
XM_024448767.1:c.175T>A	XP_024304535.1:p.Leu59Ile
XR_001748034.2:n.720T>A
NM_001363563.2:c.436T>A	NP_001350492.1:p.Leu146Ile
NM_006028.5:c.469T>A MANE Select	NP_006019.1:p.Leu157Ile