Canonical Allele Identifier: CA671975573

Gene: HTR3B

Linked Data

• dbSNP Id: rs1292729480
• gnomAD v3: 11-113932183-T-C
• gnomAD v4: 11-113932183-T-C
• MyVariant Identifiers: chr11:g.113802905T>C (hg19) ; chr11:g.113932183T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932183T>C , CM000673.2:g.113932183T>C	GRCh38
NC_000011.9:g.113802905T>C , CM000673.1:g.113802905T>C	GRCh37
NC_000011.8:g.113308115T>C	NCBI36
NG_011483.1:g.32317T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.369-106T>C MANE Select	ENSP00000260191.2:n.369-106T>C
ENST00000260191.7:c.369-106T>C	ENSP00000260191.2:n.369-106T>C
ENST00000260191.6:c.369-106T>C	ENSP00000260191.2:n.369-106T>C
ENST00000537778.5:c.336-106T>C	ENSP00000443118.1:n.336-106T>C
ENST00000543092.1:c.155-106T>C
NM_006028.4:c.369-106T>C	NP_006019.1:n.369-106T>C
XM_011543063.1:c.336-106T>C	XP_011541365.1:n.336-106T>C
XM_011543064.1:c.168-106T>C	XP_011541366.1:n.168-106T>C
XM_011543065.1:c.162-106T>C	XP_011541367.1:n.162-106T>C
XM_011543066.1:c.336-106T>C	XP_011541368.1:n.336-106T>C
NM_001363563.1:c.336-106T>C	NP_001350492.1:n.336-106T>C
XM_017018552.2:c.162-106T>C	XP_016874041.1:n.162-106T>C
XM_024448767.1:c.75-106T>C	XP_024304535.1:n.75-106T>C
XR_001748034.2:n.620-106T>C
NM_001363563.2:c.336-106T>C	NP_001350492.1:n.336-106T>C
NM_006028.5:c.369-106T>C MANE Select	NP_006019.1:n.369-106T>C