Canonical Allele Identifier: CA2001398127

Gene: HTR3B

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932694_113932695delinsTC , CM000673.2:g.113932694_113932695delinsTC	GRCh38
NC_000011.9:g.113803416_113803417delinsTC , CM000673.1:g.113803416_113803417delinsTC	GRCh37
NC_000011.8:g.113308626_113308627delinsTC	NCBI36
NG_011483.1:g.32828_32829delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+236_538+237delinsTC MANE Select	ENSP00000260191.2:n.538+236_538+237delinsTC
ENST00000260191.7:c.538+236_538+237delinsTC	ENSP00000260191.2:n.538+236_538+237delinsTC
ENST00000260191.6:c.538+236_538+237delinsTC	ENSP00000260191.2:n.538+236_538+237delinsTC
ENST00000537778.5:c.505+236_505+237delinsTC	ENSP00000443118.1:n.505+236_505+237delinsTC
ENST00000543092.1:c.324+236_324+237delinsTC
NM_006028.4:c.538+236_538+237delinsTC	NP_006019.1:n.538+236_538+237delinsTC
XM_011543063.1:c.505+236_505+237delinsTC	XP_011541365.1:n.505+236_505+237delinsTC
XM_011543064.1:c.337+236_337+237delinsTC	XP_011541366.1:n.337+236_337+237delinsTC
XM_011543065.1:c.331+236_331+237delinsTC	XP_011541367.1:n.331+236_331+237delinsTC
XM_011543066.1:c.505+236_505+237delinsTC	XP_011541368.1:n.505+236_505+237delinsTC
NM_001363563.1:c.505+236_505+237delinsTC	NP_001350492.1:n.505+236_505+237delinsTC
XM_017018552.2:c.331+236_331+237delinsTC	XP_016874041.1:n.331+236_331+237delinsTC
XM_024448767.1:c.244+236_244+237delinsTC	XP_024304535.1:n.244+236_244+237delinsTC
XR_001748034.2:n.789+236_789+237delinsTC
NM_001363563.2:c.505+236_505+237delinsTC	NP_001350492.1:n.505+236_505+237delinsTC
NM_006028.5:c.538+236_538+237delinsTC MANE Select	NP_006019.1:n.538+236_538+237delinsTC