Canonical Allele Identifier: CA382668664

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803027T>A (hg19) ; chr11:g.113932305T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932305T>A , CM000673.2:g.113932305T>A	GRCh38
NC_000011.9:g.113803027T>A , CM000673.1:g.113803027T>A	GRCh37
NC_000011.8:g.113308237T>A	NCBI36
NG_011483.1:g.32439T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.385T>A MANE Select	ENSP00000260191.2:p.Tyr129Asn
ENST00000260191.7:c.385T>A	ENSP00000260191.2:p.Tyr129Asn
ENST00000260191.6:c.385T>A	ENSP00000260191.2:p.Tyr129Asn
ENST00000537778.5:c.352T>A	ENSP00000443118.1:p.Tyr118Asn
ENST00000543092.1:c.171T>A
NM_006028.4:c.385T>A	NP_006019.1:p.Tyr129Asn
XM_011543063.1:c.352T>A	XP_011541365.1:p.Tyr118Asn
XM_011543064.1:c.184T>A	XP_011541366.1:p.Tyr62Asn
XM_011543065.1:c.178T>A	XP_011541367.1:p.Tyr60Asn
XM_011543066.1:c.352T>A	XP_011541368.1:p.Tyr118Asn
NM_001363563.1:c.352T>A	NP_001350492.1:p.Tyr118Asn
XM_017018552.2:c.178T>A	XP_016874041.1:p.Tyr60Asn
XM_024448767.1:c.91T>A	XP_024304535.1:p.Tyr31Asn
XR_001748034.2:n.636T>A
NM_001363563.2:c.352T>A	NP_001350492.1:p.Tyr118Asn
NM_006028.5:c.385T>A MANE Select	NP_006019.1:p.Tyr129Asn