Canonical Allele Identifier: CA382668892

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803091A>C (hg19) ; chr11:g.113932369A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932369A>C , CM000673.2:g.113932369A>C	GRCh38
NC_000011.9:g.113803091A>C , CM000673.1:g.113803091A>C	GRCh37
NC_000011.8:g.113308301A>C	NCBI36
NG_011483.1:g.32503A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.449A>C MANE Select	ENSP00000260191.2:p.Gln150Pro
ENST00000260191.7:c.449A>C	ENSP00000260191.2:p.Gln150Pro
ENST00000260191.6:c.449A>C	ENSP00000260191.2:p.Gln150Pro
ENST00000537778.5:c.416A>C	ENSP00000443118.1:p.Gln139Pro
ENST00000543092.1:c.235A>C
NM_006028.4:c.449A>C	NP_006019.1:p.Gln150Pro
XM_011543063.1:c.416A>C	XP_011541365.1:p.Gln139Pro
XM_011543064.1:c.248A>C	XP_011541366.1:p.Gln83Pro
XM_011543065.1:c.242A>C	XP_011541367.1:p.Gln81Pro
XM_011543066.1:c.416A>C	XP_011541368.1:p.Gln139Pro
NM_001363563.1:c.416A>C	NP_001350492.1:p.Gln139Pro
XM_017018552.2:c.242A>C	XP_016874041.1:p.Gln81Pro
XM_024448767.1:c.155A>C	XP_024304535.1:p.Gln52Pro
XR_001748034.2:n.700A>C
NM_001363563.2:c.416A>C	NP_001350492.1:p.Gln139Pro
NM_006028.5:c.449A>C MANE Select	NP_006019.1:p.Gln150Pro