Canonical Allele Identifier: CA382668573

Gene: HTR3B

Linked Data

• dbSNP Id: rs1950043375
• gnomAD v4: 11-113932290-G-A
• MyVariant Identifiers: chr11:g.113803012G>A (hg19) ; chr11:g.113932290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932290G>A , CM000673.2:g.113932290G>A	GRCh38
NC_000011.9:g.113803012G>A , CM000673.1:g.113803012G>A	GRCh37
NC_000011.8:g.113308222G>A	NCBI36
NG_011483.1:g.32424G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.370G>A MANE Select	ENSP00000260191.2:p.Val124Met
ENST00000260191.7:c.370G>A	ENSP00000260191.2:p.Val124Met
ENST00000260191.6:c.370G>A	ENSP00000260191.2:p.Val124Met
ENST00000537778.5:c.337G>A	ENSP00000443118.1:p.Val113Met
ENST00000543092.1:c.156G>A
NM_006028.4:c.370G>A	NP_006019.1:p.Val124Met
XM_011543063.1:c.337G>A	XP_011541365.1:p.Val113Met
XM_011543064.1:c.169G>A	XP_011541366.1:p.Val57Met
XM_011543065.1:c.163G>A	XP_011541367.1:p.Val55Met
XM_011543066.1:c.337G>A	XP_011541368.1:p.Val113Met
NM_001363563.1:c.337G>A	NP_001350492.1:p.Val113Met
XM_017018552.2:c.163G>A	XP_016874041.1:p.Val55Met
XM_024448767.1:c.76G>A	XP_024304535.1:p.Val26Met
XR_001748034.2:n.621G>A
NM_001363563.2:c.337G>A	NP_001350492.1:p.Val113Met
NM_006028.5:c.370G>A MANE Select	NP_006019.1:p.Val124Met