Canonical Allele Identifier: CA382668808

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803063G>C (hg19) ; chr11:g.113932341G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932341G>C , CM000673.2:g.113932341G>C	GRCh38
NC_000011.9:g.113803063G>C , CM000673.1:g.113803063G>C	GRCh37
NC_000011.8:g.113308273G>C	NCBI36
NG_011483.1:g.32475G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.421G>C MANE Select	ENSP00000260191.2:p.Gly141Arg
ENST00000260191.7:c.421G>C	ENSP00000260191.2:p.Gly141Arg
ENST00000260191.6:c.421G>C	ENSP00000260191.2:p.Gly141Arg
ENST00000537778.5:c.388G>C	ENSP00000443118.1:p.Gly130Arg
ENST00000543092.1:c.207G>C
NM_006028.4:c.421G>C	NP_006019.1:p.Gly141Arg
XM_011543063.1:c.388G>C	XP_011541365.1:p.Gly130Arg
XM_011543064.1:c.220G>C	XP_011541366.1:p.Gly74Arg
XM_011543065.1:c.214G>C	XP_011541367.1:p.Gly72Arg
XM_011543066.1:c.388G>C	XP_011541368.1:p.Gly130Arg
NM_001363563.1:c.388G>C	NP_001350492.1:p.Gly130Arg
XM_017018552.2:c.214G>C	XP_016874041.1:p.Gly72Arg
XM_024448767.1:c.127G>C	XP_024304535.1:p.Gly43Arg
XR_001748034.2:n.672G>C
NM_001363563.2:c.388G>C	NP_001350492.1:p.Gly130Arg
NM_006028.5:c.421G>C MANE Select	NP_006019.1:p.Gly141Arg