Canonical Allele Identifier: CA6284036

Gene: HTR3B

Linked Data

• ClinVar Variation Id: 790848
• ClinVar RCV Id: RCV000973707
• dbSNP Id: rs11214773
• ExAC: 11:113803008 T / C
• gnomAD v2: 11-113803008-T-C
• gnomAD v3: 11-113932286-T-C
• gnomAD v4: 11-113932286-T-C
• MyVariant Identifiers: chr11:g.113803008T>C (hg19) ; chr11:g.113932286T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932286T>C , CM000673.2:g.113932286T>C	GRCh38
NC_000011.9:g.113803008T>C , CM000673.1:g.113803008T>C	GRCh37
NC_000011.8:g.113308218T>C	NCBI36
NG_011483.1:g.32420T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.369-3T>C MANE Select	ENSP00000260191.2:n.369-3T>C
ENST00000260191.7:c.369-3T>C	ENSP00000260191.2:n.369-3T>C
ENST00000260191.6:c.369-3T>C	ENSP00000260191.2:n.369-3T>C
ENST00000537778.5:c.336-3T>C	ENSP00000443118.1:n.336-3T>C
ENST00000543092.1:c.155-3T>C
NM_006028.4:c.369-3T>C	NP_006019.1:n.369-3T>C
XM_011543063.1:c.336-3T>C	XP_011541365.1:n.336-3T>C
XM_011543064.1:c.168-3T>C	XP_011541366.1:n.168-3T>C
XM_011543065.1:c.162-3T>C	XP_011541367.1:n.162-3T>C
XM_011543066.1:c.336-3T>C	XP_011541368.1:n.336-3T>C
NM_001363563.1:c.336-3T>C	NP_001350492.1:n.336-3T>C
XM_017018552.2:c.162-3T>C	XP_016874041.1:n.162-3T>C
XM_024448767.1:c.75-3T>C	XP_024304535.1:n.75-3T>C
XR_001748034.2:n.620-3T>C
NM_001363563.2:c.336-3T>C	NP_001350492.1:n.336-3T>C
NM_006028.5:c.369-3T>C MANE Select	NP_006019.1:n.369-3T>C