Canonical Allele Identifier: CA382668597

Gene: HTR3B

Linked Data

• dbSNP Id: rs1196396208
• gnomAD v4: 11-113932294-A-G
• MyVariant Identifiers: chr11:g.113803016A>G (hg19) ; chr11:g.113932294A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932294A>G , CM000673.2:g.113932294A>G	GRCh38
NC_000011.9:g.113803016A>G , CM000673.1:g.113803016A>G	GRCh37
NC_000011.8:g.113308226A>G	NCBI36
NG_011483.1:g.32428A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.374A>G MANE Select	ENSP00000260191.2:p.Asp125Gly
ENST00000260191.7:c.374A>G	ENSP00000260191.2:p.Asp125Gly
ENST00000260191.6:c.374A>G	ENSP00000260191.2:p.Asp125Gly
ENST00000537778.5:c.341A>G	ENSP00000443118.1:p.Asp114Gly
ENST00000543092.1:c.160A>G
NM_006028.4:c.374A>G	NP_006019.1:p.Asp125Gly
XM_011543063.1:c.341A>G	XP_011541365.1:p.Asp114Gly
XM_011543064.1:c.173A>G	XP_011541366.1:p.Asp58Gly
XM_011543065.1:c.167A>G	XP_011541367.1:p.Asp56Gly
XM_011543066.1:c.341A>G	XP_011541368.1:p.Asp114Gly
NM_001363563.1:c.341A>G	NP_001350492.1:p.Asp114Gly
XM_017018552.2:c.167A>G	XP_016874041.1:p.Asp56Gly
XM_024448767.1:c.80A>G	XP_024304535.1:p.Asp27Gly
XR_001748034.2:n.625A>G
NM_001363563.2:c.341A>G	NP_001350492.1:p.Asp114Gly
NM_006028.5:c.374A>G MANE Select	NP_006019.1:p.Asp125Gly