Canonical Allele Identifier: CA382668776

Gene: HTR3B

Linked Data

• ClinVar Variation Id: 2606080
• ClinVar RCV Id: RCV004344694
• dbSNP Id: rs1181939895
• gnomAD v2: 11-113803049-A-G
• gnomAD v3: 11-113932327-A-G
• gnomAD v4: 11-113932327-A-G
• MyVariant Identifiers: chr11:g.113803049A>G (hg19) ; chr11:g.113932327A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932327A>G , CM000673.2:g.113932327A>G	GRCh38
NC_000011.9:g.113803049A>G , CM000673.1:g.113803049A>G	GRCh37
NC_000011.8:g.113308259A>G	NCBI36
NG_011483.1:g.32461A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.407A>G MANE Select	ENSP00000260191.2:p.Tyr136Cys
ENST00000260191.7:c.407A>G	ENSP00000260191.2:p.Tyr136Cys
ENST00000260191.6:c.407A>G	ENSP00000260191.2:p.Tyr136Cys
ENST00000537778.5:c.374A>G	ENSP00000443118.1:p.Tyr125Cys
ENST00000543092.1:c.193A>G
NM_006028.4:c.407A>G	NP_006019.1:p.Tyr136Cys
XM_011543063.1:c.374A>G	XP_011541365.1:p.Tyr125Cys
XM_011543064.1:c.206A>G	XP_011541366.1:p.Tyr69Cys
XM_011543065.1:c.200A>G	XP_011541367.1:p.Tyr67Cys
XM_011543066.1:c.374A>G	XP_011541368.1:p.Tyr125Cys
NM_001363563.1:c.374A>G	NP_001350492.1:p.Tyr125Cys
XM_017018552.2:c.200A>G	XP_016874041.1:p.Tyr67Cys
XM_024448767.1:c.113A>G	XP_024304535.1:p.Tyr38Cys
XR_001748034.2:n.658A>G
NM_001363563.2:c.374A>G	NP_001350492.1:p.Tyr125Cys
NM_006028.5:c.407A>G MANE Select	NP_006019.1:p.Tyr136Cys