Canonical Allele Identifier: CA228668011

Gene: HTR3B

Linked Data

• dbSNP Id: rs1019026918
• MyVariant Identifiers: chr11:g.113803106G>C (hg19) ; chr11:g.113932384G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932384G>C , CM000673.2:g.113932384G>C	GRCh38
NC_000011.9:g.113803106G>C , CM000673.1:g.113803106G>C	GRCh37
NC_000011.8:g.113308316G>C	NCBI36
NG_011483.1:g.32518G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.464G>C MANE Select	ENSP00000260191.2:p.Cys155Ser
ENST00000260191.7:c.464G>C	ENSP00000260191.2:p.Cys155Ser
ENST00000260191.6:c.464G>C	ENSP00000260191.2:p.Cys155Ser
ENST00000537778.5:c.431G>C	ENSP00000443118.1:p.Cys144Ser
ENST00000543092.1:c.250G>C
NM_006028.4:c.464G>C	NP_006019.1:p.Cys155Ser
XM_011543063.1:c.431G>C	XP_011541365.1:p.Cys144Ser
XM_011543064.1:c.263G>C	XP_011541366.1:p.Cys88Ser
XM_011543065.1:c.257G>C	XP_011541367.1:p.Cys86Ser
XM_011543066.1:c.431G>C	XP_011541368.1:p.Cys144Ser
NM_001363563.1:c.431G>C	NP_001350492.1:p.Cys144Ser
XM_017018552.2:c.257G>C	XP_016874041.1:p.Cys86Ser
XM_024448767.1:c.170G>C	XP_024304535.1:p.Cys57Ser
XR_001748034.2:n.715G>C
NM_001363563.2:c.431G>C	NP_001350492.1:p.Cys144Ser
NM_006028.5:c.464G>C MANE Select	NP_006019.1:p.Cys155Ser