Canonical Allele Identifier: CA382668583

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803013T>C (hg19) ; chr11:g.113932291T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932291T>C , CM000673.2:g.113932291T>C	GRCh38
NC_000011.9:g.113803013T>C , CM000673.1:g.113803013T>C	GRCh37
NC_000011.8:g.113308223T>C	NCBI36
NG_011483.1:g.32425T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.371T>C MANE Select	ENSP00000260191.2:p.Val124Ala
ENST00000260191.7:c.371T>C	ENSP00000260191.2:p.Val124Ala
ENST00000260191.6:c.371T>C	ENSP00000260191.2:p.Val124Ala
ENST00000537778.5:c.338T>C	ENSP00000443118.1:p.Val113Ala
ENST00000543092.1:c.157T>C
NM_006028.4:c.371T>C	NP_006019.1:p.Val124Ala
XM_011543063.1:c.338T>C	XP_011541365.1:p.Val113Ala
XM_011543064.1:c.170T>C	XP_011541366.1:p.Val57Ala
XM_011543065.1:c.164T>C	XP_011541367.1:p.Val55Ala
XM_011543066.1:c.338T>C	XP_011541368.1:p.Val113Ala
NM_001363563.1:c.338T>C	NP_001350492.1:p.Val113Ala
XM_017018552.2:c.164T>C	XP_016874041.1:p.Val55Ala
XM_024448767.1:c.77T>C	XP_024304535.1:p.Val26Ala
XR_001748034.2:n.622T>C
NM_001363563.2:c.338T>C	NP_001350492.1:p.Val113Ala
NM_006028.5:c.371T>C MANE Select	NP_006019.1:p.Val124Ala