Canonical Allele Identifier: CA382669269

Gene: HTR3B

Linked Data

• MyVariant Identifiers: chr11:g.113803169T>A (hg19) ; chr11:g.113932447T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932447T>A , CM000673.2:g.113932447T>A	GRCh38
NC_000011.9:g.113803169T>A , CM000673.1:g.113803169T>A	GRCh37
NC_000011.8:g.113308379T>A	NCBI36
NG_011483.1:g.32581T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.527T>A MANE Select	ENSP00000260191.2:p.Ile176Asn
ENST00000260191.7:c.527T>A	ENSP00000260191.2:p.Ile176Asn
ENST00000260191.6:c.527T>A	ENSP00000260191.2:p.Ile176Asn
ENST00000537778.5:c.494T>A	ENSP00000443118.1:p.Ile165Asn
ENST00000543092.1:c.313T>A
NM_006028.4:c.527T>A	NP_006019.1:p.Ile176Asn
XM_011543063.1:c.494T>A	XP_011541365.1:p.Ile165Asn
XM_011543064.1:c.326T>A	XP_011541366.1:p.Ile109Asn
XM_011543065.1:c.320T>A	XP_011541367.1:p.Ile107Asn
XM_011543066.1:c.494T>A	XP_011541368.1:p.Ile165Asn
NM_001363563.1:c.494T>A	NP_001350492.1:p.Ile165Asn
XM_017018552.2:c.320T>A	XP_016874041.1:p.Ile107Asn
XM_024448767.1:c.233T>A	XP_024304535.1:p.Ile78Asn
XR_001748034.2:n.778T>A
NM_001363563.2:c.494T>A	NP_001350492.1:p.Ile165Asn
NM_006028.5:c.527T>A MANE Select	NP_006019.1:p.Ile176Asn