Canonical Allele Identifier: CA13429354

Gene: HTR3B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113942011G>A , CM000673.2:g.113942011G>A	GRCh38
NC_000011.9:g.113812733G>A , CM000673.1:g.113812733G>A	GRCh37
NC_000011.8:g.113317943G>A	NCBI36
NG_011483.1:g.42145G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.697-971G>A MANE Select	ENSP00000260191.2:n.697-971G>A
ENST00000260191.7:c.697-971G>A	ENSP00000260191.2:n.697-971G>A
ENST00000260191.6:c.697-971G>A	ENSP00000260191.2:n.697-971G>A
ENST00000537778.5:c.664-971G>A	ENSP00000443118.1:n.664-971G>A
ENST00000543092.1:c.483-2562G>A
NM_006028.4:c.697-971G>A	NP_006019.1:n.697-971G>A
XM_011543063.1:c.664-971G>A	XP_011541365.1:n.664-971G>A
XM_011543064.1:c.496-971G>A	XP_011541366.1:n.496-971G>A
XM_011543065.1:c.490-971G>A	XP_011541367.1:n.490-971G>A
XM_011543066.1:c.664-2562G>A	XP_011541368.1:n.664-2562G>A
NM_001363563.1:c.664-971G>A	NP_001350492.1:n.664-971G>A
XM_017018552.2:c.490-971G>A	XP_016874041.1:n.490-971G>A
XM_024448767.1:c.403-971G>A	XP_024304535.1:n.403-971G>A
XR_001748034.2:n.948-2562G>A
NM_001363563.2:c.664-971G>A	NP_001350492.1:n.664-971G>A
NM_006028.5:c.697-971G>A MANE Select	NP_006019.1:n.697-971G>A