Canonical Allele Identifier: CA2616054435

Gene: HTR3B

Linked Data

• gnomAD v4: 11-113932458-G-GTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113932458_113932459insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA , CM000673.2:g.113932458_113932459insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA	GRCh38
NC_000011.9:g.113803180_113803181insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA , CM000673.1:g.113803180_113803181insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA	GRCh37
NC_000011.8:g.113308390_113308391insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA	NCBI36
NG_011483.1:g.32592_32593insTGGAAGACATAGACCTGGCCTTTCTGAGGAGCCCAGAA

Transcript Alleles

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