Canonical Allele Identifier: CA382668590

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803015G>C (hg19) ; chr11:g.113932293G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932293G>C , CM000673.2:g.113932293G>C	GRCh38
NC_000011.9:g.113803015G>C , CM000673.1:g.113803015G>C	GRCh37
NC_000011.8:g.113308225G>C	NCBI36
NG_011483.1:g.32427G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.373G>C MANE Select	ENSP00000260191.2:p.Asp125His
ENST00000260191.7:c.373G>C	ENSP00000260191.2:p.Asp125His
ENST00000260191.6:c.373G>C	ENSP00000260191.2:p.Asp125His
ENST00000537778.5:c.340G>C	ENSP00000443118.1:p.Asp114His
ENST00000543092.1:c.159G>C
NM_006028.4:c.373G>C	NP_006019.1:p.Asp125His
XM_011543063.1:c.340G>C	XP_011541365.1:p.Asp114His
XM_011543064.1:c.172G>C	XP_011541366.1:p.Asp58His
XM_011543065.1:c.166G>C	XP_011541367.1:p.Asp56His
XM_011543066.1:c.340G>C	XP_011541368.1:p.Asp114His
NM_001363563.1:c.340G>C	NP_001350492.1:p.Asp114His
XM_017018552.2:c.166G>C	XP_016874041.1:p.Asp56His
XM_024448767.1:c.79G>C	XP_024304535.1:p.Asp27His
XR_001748034.2:n.624G>C
NM_001363563.2:c.340G>C	NP_001350492.1:p.Asp114His
NM_006028.5:c.373G>C MANE Select	NP_006019.1:p.Asp125His