Canonical Allele Identifier: CA382668861

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803082A>T (hg19) ; chr11:g.113932360A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932360A>T , CM000673.2:g.113932360A>T	GRCh38
NC_000011.9:g.113803082A>T , CM000673.1:g.113803082A>T	GRCh37
NC_000011.8:g.113308292A>T	NCBI36
NG_011483.1:g.32494A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.440A>T MANE Select	ENSP00000260191.2:p.Lys147Met
ENST00000260191.7:c.440A>T	ENSP00000260191.2:p.Lys147Met
ENST00000260191.6:c.440A>T	ENSP00000260191.2:p.Lys147Met
ENST00000537778.5:c.407A>T	ENSP00000443118.1:p.Lys136Met
ENST00000543092.1:c.226A>T
NM_006028.4:c.440A>T	NP_006019.1:p.Lys147Met
XM_011543063.1:c.407A>T	XP_011541365.1:p.Lys136Met
XM_011543064.1:c.239A>T	XP_011541366.1:p.Lys80Met
XM_011543065.1:c.233A>T	XP_011541367.1:p.Lys78Met
XM_011543066.1:c.407A>T	XP_011541368.1:p.Lys136Met
NM_001363563.1:c.407A>T	NP_001350492.1:p.Lys136Met
XM_017018552.2:c.233A>T	XP_016874041.1:p.Lys78Met
XM_024448767.1:c.146A>T	XP_024304535.1:p.Lys49Met
XR_001748034.2:n.691A>T
NM_001363563.2:c.407A>T	NP_001350492.1:p.Lys136Met
NM_006028.5:c.440A>T MANE Select	NP_006019.1:p.Lys147Met