Canonical Allele Identifier: CA382668612

Gene: HTR3B

Linked Data

• dbSNP Id: rs1339311562
• gnomAD v3: 11-113932297-T-C
• gnomAD v4: 11-113932297-T-C
• MyVariant Identifiers: chr11:g.113803019T>C (hg19) ; chr11:g.113932297T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932297T>C , CM000673.2:g.113932297T>C	GRCh38
NC_000011.9:g.113803019T>C , CM000673.1:g.113803019T>C	GRCh37
NC_000011.8:g.113308229T>C	NCBI36
NG_011483.1:g.32431T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.377T>C MANE Select	ENSP00000260191.2:p.Ile126Thr
ENST00000260191.7:c.377T>C	ENSP00000260191.2:p.Ile126Thr
ENST00000260191.6:c.377T>C	ENSP00000260191.2:p.Ile126Thr
ENST00000537778.5:c.344T>C	ENSP00000443118.1:p.Ile115Thr
ENST00000543092.1:c.163T>C
NM_006028.4:c.377T>C	NP_006019.1:p.Ile126Thr
XM_011543063.1:c.344T>C	XP_011541365.1:p.Ile115Thr
XM_011543064.1:c.176T>C	XP_011541366.1:p.Ile59Thr
XM_011543065.1:c.170T>C	XP_011541367.1:p.Ile57Thr
XM_011543066.1:c.344T>C	XP_011541368.1:p.Ile115Thr
NM_001363563.1:c.344T>C	NP_001350492.1:p.Ile115Thr
XM_017018552.2:c.170T>C	XP_016874041.1:p.Ile57Thr
XM_024448767.1:c.83T>C	XP_024304535.1:p.Ile28Thr
XR_001748034.2:n.628T>C
NM_001363563.2:c.344T>C	NP_001350492.1:p.Ile115Thr
NM_006028.5:c.377T>C MANE Select	NP_006019.1:p.Ile126Thr