Canonical Allele Identifier: CA6284067

Gene: HTR3B

Linked Data

• dbSNP Id: rs748645127
• ExAC: 11:113803174 C / T
• gnomAD v2: 11-113803174-C-T
• gnomAD v4: 11-113932452-C-T
• MyVariant Identifiers: chr11:g.113803174C>T (hg19) ; chr11:g.113932452C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932452C>T , CM000673.2:g.113932452C>T	GRCh38
NC_000011.9:g.113803174C>T , CM000673.1:g.113803174C>T	GRCh37
NC_000011.8:g.113308384C>T	NCBI36
NG_011483.1:g.32586C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.532C>T MANE Select	ENSP00000260191.2:p.His178Tyr
ENST00000260191.7:c.532C>T	ENSP00000260191.2:p.His178Tyr
ENST00000260191.6:c.532C>T	ENSP00000260191.2:p.His178Tyr
ENST00000537778.5:c.499C>T	ENSP00000443118.1:p.His167Tyr
ENST00000543092.1:c.318C>T
NM_006028.4:c.532C>T	NP_006019.1:p.His178Tyr
XM_011543063.1:c.499C>T	XP_011541365.1:p.His167Tyr
XM_011543064.1:c.331C>T	XP_011541366.1:p.His111Tyr
XM_011543065.1:c.325C>T	XP_011541367.1:p.His109Tyr
XM_011543066.1:c.499C>T	XP_011541368.1:p.His167Tyr
NM_001363563.1:c.499C>T	NP_001350492.1:p.His167Tyr
XM_017018552.2:c.325C>T	XP_016874041.1:p.His109Tyr
XM_024448767.1:c.238C>T	XP_024304535.1:p.His80Tyr
XR_001748034.2:n.783C>T
NM_001363563.2:c.499C>T	NP_001350492.1:p.His167Tyr
NM_006028.5:c.532C>T MANE Select	NP_006019.1:p.His178Tyr