Canonical Allele Identifier: CA382668579

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803012G>C (hg19) ; chr11:g.113932290G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932290G>C , CM000673.2:g.113932290G>C	GRCh38
NC_000011.9:g.113803012G>C , CM000673.1:g.113803012G>C	GRCh37
NC_000011.8:g.113308222G>C	NCBI36
NG_011483.1:g.32424G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.370G>C MANE Select	ENSP00000260191.2:p.Val124Leu
ENST00000260191.7:c.370G>C	ENSP00000260191.2:p.Val124Leu
ENST00000260191.6:c.370G>C	ENSP00000260191.2:p.Val124Leu
ENST00000537778.5:c.337G>C	ENSP00000443118.1:p.Val113Leu
ENST00000543092.1:c.156G>C
NM_006028.4:c.370G>C	NP_006019.1:p.Val124Leu
XM_011543063.1:c.337G>C	XP_011541365.1:p.Val113Leu
XM_011543064.1:c.169G>C	XP_011541366.1:p.Val57Leu
XM_011543065.1:c.163G>C	XP_011541367.1:p.Val55Leu
XM_011543066.1:c.337G>C	XP_011541368.1:p.Val113Leu
NM_001363563.1:c.337G>C	NP_001350492.1:p.Val113Leu
XM_017018552.2:c.163G>C	XP_016874041.1:p.Val55Leu
XM_024448767.1:c.76G>C	XP_024304535.1:p.Val26Leu
XR_001748034.2:n.621G>C
NM_001363563.2:c.337G>C	NP_001350492.1:p.Val113Leu
NM_006028.5:c.370G>C MANE Select	NP_006019.1:p.Val124Leu