Canonical Allele Identifier: CA476831205

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803059A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932337A>G , CM000673.2:g.113932337A>G	GRCh38
NC_000011.9:g.113803059A>G , CM000673.1:g.113803059A>G	GRCh37
NC_000011.8:g.113308269A>G	NCBI36
NG_011483.1:g.32471A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.417A>G MANE Select	ENSP00000260191.2:p.Ser139=
ENST00000260191.7:c.417A>G	ENSP00000260191.2:p.Ser139=
ENST00000260191.6:c.417A>G	ENSP00000260191.2:p.Ser139=
ENST00000537778.5:c.384A>G	ENSP00000443118.1:p.Ser128=
ENST00000543092.1:c.203A>G
NM_006028.4:c.417A>G	NP_006019.1:p.Ser139=
XM_011543063.1:c.384A>G	XP_011541365.1:p.Ser128=
XM_011543064.1:c.216A>G	XP_011541366.1:p.Ser72=
XM_011543065.1:c.210A>G	XP_011541367.1:p.Ser70=
XM_011543066.1:c.384A>G	XP_011541368.1:p.Ser128=
NM_001363563.1:c.384A>G	NP_001350492.1:p.Ser128=
XM_017018552.2:c.210A>G	XP_016874041.1:p.Ser70=
XM_024448767.1:c.123A>G	XP_024304535.1:p.Ser41=
XR_001748034.2:n.668A>G
NM_001363563.2:c.384A>G	NP_001350492.1:p.Ser128=
NM_006028.5:c.417A>G MANE Select	NP_006019.1:p.Ser139=