Canonical Allele Identifier: CA2001382888

Gene: HTR3B

Linked Data

• dbSNP Id: rs1949776582

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910196_113910199del , CM000673.2:g.113910196_113910199del	GRCh38
NC_000011.9:g.113780918_113780921del , CM000673.1:g.113780918_113780921del	GRCh37
NC_000011.8:g.113286128_113286131del	NCBI36
NG_011483.1:g.10330_10333del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+741_213+744del MANE Select	ENSP00000260191.2:n.213+741_213+744del
ENST00000260191.7:c.213+741_213+744del	ENSP00000260191.2:n.213+741_213+744del
ENST00000260191.6:c.213+741_213+744del	ENSP00000260191.2:n.213+741_213+744del
ENST00000537778.5:c.180+741_180+744del	ENSP00000443118.1:n.180+741_180+744del
NM_006028.4:c.213+741_213+744del	NP_006019.1:n.213+741_213+744del
XM_011543063.1:c.180+741_180+744del	XP_011541365.1:n.180+741_180+744del
XM_011543064.1:c.12+11113_12+11116del	XP_011541366.1:n.12+11113_12+11116del
XM_011543066.1:c.180+741_180+744del	XP_011541368.1:n.180+741_180+744del
NM_001363563.1:c.180+741_180+744del	NP_001350492.1:n.180+741_180+744del
XM_024448767.1:c.-82+741_-82+744del	XP_024304535.1:n.-82+741_-82+744del
XR_001748034.2:n.464+741_464+744del
NM_001363563.2:c.180+741_180+744del	NP_001350492.1:n.180+741_180+744del
NM_006028.5:c.213+741_213+744del MANE Select	NP_006019.1:n.213+741_213+744del