Canonical Allele Identifier: CA6284056

Gene: HTR3B

Linked Data

• dbSNP Id: rs180672312
• ExAC: 11:113803105 T / G
• gnomAD v2: 11-113803105-T-G
• gnomAD v3: 11-113932383-T-G
• gnomAD v4: 11-113932383-T-G
• MyVariant Identifiers: chr11:g.113803105T>G (hg19) ; chr11:g.113932383T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932383T>G , CM000673.2:g.113932383T>G	GRCh38
NC_000011.9:g.113803105T>G , CM000673.1:g.113803105T>G	GRCh37
NC_000011.8:g.113308315T>G	NCBI36
NG_011483.1:g.32517T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.463T>G MANE Select	ENSP00000260191.2:p.Cys155Gly
ENST00000260191.7:c.463T>G	ENSP00000260191.2:p.Cys155Gly
ENST00000260191.6:c.463T>G	ENSP00000260191.2:p.Cys155Gly
ENST00000537778.5:c.430T>G	ENSP00000443118.1:p.Cys144Gly
ENST00000543092.1:c.249T>G
NM_006028.4:c.463T>G	NP_006019.1:p.Cys155Gly
XM_011543063.1:c.430T>G	XP_011541365.1:p.Cys144Gly
XM_011543064.1:c.262T>G	XP_011541366.1:p.Cys88Gly
XM_011543065.1:c.256T>G	XP_011541367.1:p.Cys86Gly
XM_011543066.1:c.430T>G	XP_011541368.1:p.Cys144Gly
NM_001363563.1:c.430T>G	NP_001350492.1:p.Cys144Gly
XM_017018552.2:c.256T>G	XP_016874041.1:p.Cys86Gly
XM_024448767.1:c.169T>G	XP_024304535.1:p.Cys57Gly
XR_001748034.2:n.714T>G
NM_001363563.2:c.430T>G	NP_001350492.1:p.Cys144Gly
NM_006028.5:c.463T>G MANE Select	NP_006019.1:p.Cys155Gly