Canonical Allele Identifier: CA476831301

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803086C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932364C>G , CM000673.2:g.113932364C>G	GRCh38
NC_000011.9:g.113803086C>G , CM000673.1:g.113803086C>G	GRCh37
NC_000011.8:g.113308296C>G	NCBI36
NG_011483.1:g.32498C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.444C>G MANE Select	ENSP00000260191.2:p.Pro148=
ENST00000260191.7:c.444C>G	ENSP00000260191.2:p.Pro148=
ENST00000260191.6:c.444C>G	ENSP00000260191.2:p.Pro148=
ENST00000537778.5:c.411C>G	ENSP00000443118.1:p.Pro137=
ENST00000543092.1:c.230C>G
NM_006028.4:c.444C>G	NP_006019.1:p.Pro148=
XM_011543063.1:c.411C>G	XP_011541365.1:p.Pro137=
XM_011543064.1:c.243C>G	XP_011541366.1:p.Pro81=
XM_011543065.1:c.237C>G	XP_011541367.1:p.Pro79=
XM_011543066.1:c.411C>G	XP_011541368.1:p.Pro137=
NM_001363563.1:c.411C>G	NP_001350492.1:p.Pro137=
XM_017018552.2:c.237C>G	XP_016874041.1:p.Pro79=
XM_024448767.1:c.150C>G	XP_024304535.1:p.Pro50=
XR_001748034.2:n.695C>G
NM_001363563.2:c.411C>G	NP_001350492.1:p.Pro137=
NM_006028.5:c.444C>G MANE Select	NP_006019.1:p.Pro148=