Canonical Allele Identifier: CA476831499

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932418-C-A
• MyVariant Identifiers: chr11:g.113803140C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932418C>A , CM000673.2:g.113932418C>A	GRCh38
NC_000011.9:g.113803140C>A , CM000673.1:g.113803140C>A	GRCh37
NC_000011.8:g.113308350C>A	NCBI36
NG_011483.1:g.32552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.498C>A MANE Select	ENSP00000260191.2:p.Val166=
ENST00000260191.7:c.498C>A	ENSP00000260191.2:p.Val166=
ENST00000260191.6:c.498C>A	ENSP00000260191.2:p.Val166=
ENST00000537778.5:c.465C>A	ENSP00000443118.1:p.Val155=
ENST00000543092.1:c.284C>A
NM_006028.4:c.498C>A	NP_006019.1:p.Val166=
XM_011543063.1:c.465C>A	XP_011541365.1:p.Val155=
XM_011543064.1:c.297C>A	XP_011541366.1:p.Val99=
XM_011543065.1:c.291C>A	XP_011541367.1:p.Val97=
XM_011543066.1:c.465C>A	XP_011541368.1:p.Val155=
NM_001363563.1:c.465C>A	NP_001350492.1:p.Val155=
XM_017018552.2:c.291C>A	XP_016874041.1:p.Val97=
XM_024448767.1:c.204C>A	XP_024304535.1:p.Val68=
XR_001748034.2:n.749C>A
NM_001363563.2:c.465C>A	NP_001350492.1:p.Val155=
NM_006028.5:c.498C>A MANE Select	NP_006019.1:p.Val166=