Canonical Allele Identifier: CA2616054449

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932497-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932497C>T , CM000673.2:g.113932497C>T	GRCh38
NC_000011.9:g.113803219C>T , CM000673.1:g.113803219C>T	GRCh37
NC_000011.8:g.113308429C>T	NCBI36
NG_011483.1:g.32631C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260191.8:c.538+39C>T MANE Select	ENSP00000260191.2:n.538+39C>T
ENST00000260191.7:c.538+39C>T	ENSP00000260191.2:n.538+39C>T
ENST00000260191.6:c.538+39C>T	ENSP00000260191.2:n.538+39C>T
ENST00000537778.5:c.505+39C>T	ENSP00000443118.1:n.505+39C>T
ENST00000543092.1:c.324+39C>T
NM_006028.4:c.538+39C>T	NP_006019.1:n.538+39C>T
XM_011543063.1:c.505+39C>T	XP_011541365.1:n.505+39C>T
XM_011543064.1:c.337+39C>T	XP_011541366.1:n.337+39C>T
XM_011543065.1:c.331+39C>T	XP_011541367.1:n.331+39C>T
XM_011543066.1:c.505+39C>T	XP_011541368.1:n.505+39C>T
NM_001363563.1:c.505+39C>T	NP_001350492.1:n.505+39C>T
XM_017018552.2:c.331+39C>T	XP_016874041.1:n.331+39C>T
XM_024448767.1:c.244+39C>T	XP_024304535.1:n.244+39C>T
XR_001748034.2:n.789+39C>T
NM_001363563.2:c.505+39C>T	NP_001350492.1:n.505+39C>T
NM_006028.5:c.538+39C>T MANE Select	NP_006019.1:n.538+39C>T