Canonical Allele Identifier: CA228668387

Gene: HTR3B

Linked Data

• dbSNP Id: rs200852873
• MyVariant Identifiers: chr11:g.113803379T>A (hg19) ; chr11:g.113932657T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932657T>A , CM000673.2:g.113932657T>A	GRCh38
NC_000011.9:g.113803379T>A , CM000673.1:g.113803379T>A	GRCh37
NC_000011.8:g.113308589T>A	NCBI36
NG_011483.1:g.32791T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+199T>A MANE Select	ENSP00000260191.2:n.538+199T>A
ENST00000260191.7:c.538+199T>A	ENSP00000260191.2:n.538+199T>A
ENST00000260191.6:c.538+199T>A	ENSP00000260191.2:n.538+199T>A
ENST00000537778.5:c.505+199T>A	ENSP00000443118.1:n.505+199T>A
ENST00000543092.1:c.324+199T>A
NM_006028.4:c.538+199T>A	NP_006019.1:n.538+199T>A
XM_011543063.1:c.505+199T>A	XP_011541365.1:n.505+199T>A
XM_011543064.1:c.337+199T>A	XP_011541366.1:n.337+199T>A
XM_011543065.1:c.331+199T>A	XP_011541367.1:n.331+199T>A
XM_011543066.1:c.505+199T>A	XP_011541368.1:n.505+199T>A
NM_001363563.1:c.505+199T>A	NP_001350492.1:n.505+199T>A
XM_017018552.2:c.331+199T>A	XP_016874041.1:n.331+199T>A
XM_024448767.1:c.244+199T>A	XP_024304535.1:n.244+199T>A
XR_001748034.2:n.789+199T>A
NM_001363563.2:c.505+199T>A	NP_001350492.1:n.505+199T>A
NM_006028.5:c.538+199T>A MANE Select	NP_006019.1:n.538+199T>A