Canonical Allele Identifier: CA671975791

Gene: HTR3B

Linked Data

• dbSNP Id: rs1445604207
• gnomAD v3: 11-113932524-C-G
• gnomAD v4: 11-113932524-C-G
• MyVariant Identifiers: chr11:g.113803246C>G (hg19) ; chr11:g.113932524C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932524C>G , CM000673.2:g.113932524C>G	GRCh38
NC_000011.9:g.113803246C>G , CM000673.1:g.113803246C>G	GRCh37
NC_000011.8:g.113308456C>G	NCBI36
NG_011483.1:g.32658C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+66C>G MANE Select	ENSP00000260191.2:n.538+66C>G
ENST00000260191.7:c.538+66C>G	ENSP00000260191.2:n.538+66C>G
ENST00000260191.6:c.538+66C>G	ENSP00000260191.2:n.538+66C>G
ENST00000537778.5:c.505+66C>G	ENSP00000443118.1:n.505+66C>G
ENST00000543092.1:c.324+66C>G
NM_006028.4:c.538+66C>G	NP_006019.1:n.538+66C>G
XM_011543063.1:c.505+66C>G	XP_011541365.1:n.505+66C>G
XM_011543064.1:c.337+66C>G	XP_011541366.1:n.337+66C>G
XM_011543065.1:c.331+66C>G	XP_011541367.1:n.331+66C>G
XM_011543066.1:c.505+66C>G	XP_011541368.1:n.505+66C>G
NM_001363563.1:c.505+66C>G	NP_001350492.1:n.505+66C>G
XM_017018552.2:c.331+66C>G	XP_016874041.1:n.331+66C>G
XM_024448767.1:c.244+66C>G	XP_024304535.1:n.244+66C>G
XR_001748034.2:n.789+66C>G
NM_001363563.2:c.505+66C>G	NP_001350492.1:n.505+66C>G
NM_006028.5:c.538+66C>G MANE Select	NP_006019.1:n.538+66C>G