Canonical Allele Identifier: CA476831408

Gene: HTR3B

Linked Data

• dbSNP Id: rs1168662465
• gnomAD v2: 11-113803113-A-G
• gnomAD v4: 11-113932391-A-G
• MyVariant Identifiers: chr11:g.113803113A>G (hg19) ; chr11:g.113932391A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932391A>G , CM000673.2:g.113932391A>G	GRCh38
NC_000011.9:g.113803113A>G , CM000673.1:g.113803113A>G	GRCh37
NC_000011.8:g.113308323A>G	NCBI36
NG_011483.1:g.32525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.471A>G MANE Select	ENSP00000260191.2:p.Leu157=
ENST00000260191.7:c.471A>G	ENSP00000260191.2:p.Leu157=
ENST00000260191.6:c.471A>G	ENSP00000260191.2:p.Leu157=
ENST00000537778.5:c.438A>G	ENSP00000443118.1:p.Leu146=
ENST00000543092.1:c.257A>G
NM_006028.4:c.471A>G	NP_006019.1:p.Leu157=
XM_011543063.1:c.438A>G	XP_011541365.1:p.Leu146=
XM_011543064.1:c.270A>G	XP_011541366.1:p.Leu90=
XM_011543065.1:c.264A>G	XP_011541367.1:p.Leu88=
XM_011543066.1:c.438A>G	XP_011541368.1:p.Leu146=
NM_001363563.1:c.438A>G	NP_001350492.1:p.Leu146=
XM_017018552.2:c.264A>G	XP_016874041.1:p.Leu88=
XM_024448767.1:c.177A>G	XP_024304535.1:p.Leu59=
XR_001748034.2:n.722A>G
NM_001363563.2:c.438A>G	NP_001350492.1:p.Leu146=
NM_006028.5:c.471A>G MANE Select	NP_006019.1:p.Leu157=