Canonical Allele Identifier: CA382668565

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803010G>T (hg19) ; chr11:g.113932288G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932288G>T , CM000673.2:g.113932288G>T	GRCh38
NC_000011.9:g.113803010G>T , CM000673.1:g.113803010G>T	GRCh37
NC_000011.8:g.113308220G>T	NCBI36
NG_011483.1:g.32422G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-1G>T MANE Select	ENSP00000260191.2:n.369-1G>T
ENST00000260191.7:c.369-1G>T	ENSP00000260191.2:n.369-1G>T
ENST00000260191.6:c.369-1G>T	ENSP00000260191.2:n.369-1G>T
ENST00000537778.5:c.336-1G>T	ENSP00000443118.1:n.336-1G>T
ENST00000543092.1:c.155-1G>T
NM_006028.4:c.369-1G>T	NP_006019.1:n.369-1G>T
XM_011543063.1:c.336-1G>T	XP_011541365.1:n.336-1G>T
XM_011543064.1:c.168-1G>T	XP_011541366.1:n.168-1G>T
XM_011543065.1:c.162-1G>T	XP_011541367.1:n.162-1G>T
XM_011543066.1:c.336-1G>T	XP_011541368.1:n.336-1G>T
NM_001363563.1:c.336-1G>T	NP_001350492.1:n.336-1G>T
XM_017018552.2:c.162-1G>T	XP_016874041.1:n.162-1G>T
XM_024448767.1:c.75-1G>T	XP_024304535.1:n.75-1G>T
XR_001748034.2:n.620-1G>T
NM_001363563.2:c.336-1G>T	NP_001350492.1:n.336-1G>T
NM_006028.5:c.369-1G>T MANE Select	NP_006019.1:n.369-1G>T