Canonical Allele Identifier: CA382668794

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932334-C-G
• MyVariant Identifiers: chr11:g.113803056C>G (hg19) ; chr11:g.113932334C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932334C>G , CM000673.2:g.113932334C>G	GRCh38
NC_000011.9:g.113803056C>G , CM000673.1:g.113803056C>G	GRCh37
NC_000011.8:g.113308266C>G	NCBI36
NG_011483.1:g.32468C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.414C>G MANE Select	ENSP00000260191.2:p.Asn138Lys
ENST00000260191.7:c.414C>G	ENSP00000260191.2:p.Asn138Lys
ENST00000260191.6:c.414C>G	ENSP00000260191.2:p.Asn138Lys
ENST00000537778.5:c.381C>G	ENSP00000443118.1:p.Asn127Lys
ENST00000543092.1:c.200C>G
NM_006028.4:c.414C>G	NP_006019.1:p.Asn138Lys
XM_011543063.1:c.381C>G	XP_011541365.1:p.Asn127Lys
XM_011543064.1:c.213C>G	XP_011541366.1:p.Asn71Lys
XM_011543065.1:c.207C>G	XP_011541367.1:p.Asn69Lys
XM_011543066.1:c.381C>G	XP_011541368.1:p.Asn127Lys
NM_001363563.1:c.381C>G	NP_001350492.1:p.Asn127Lys
XM_017018552.2:c.207C>G	XP_016874041.1:p.Asn69Lys
XM_024448767.1:c.120C>G	XP_024304535.1:p.Asn40Lys
XR_001748034.2:n.665C>G
NM_001363563.2:c.381C>G	NP_001350492.1:p.Asn127Lys
NM_006028.5:c.414C>G MANE Select	NP_006019.1:p.Asn138Lys