Canonical Allele Identifier: CA942406438

Gene: HTR3B

Linked Data

• dbSNP Id: rs1949774401
• gnomAD v3: 11-113910153-AAG-A
• gnomAD v4: 11-113910153-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113910159_113910160del , CM000673.2:g.113910159_113910160del	GRCh38
NC_000011.9:g.113780881_113780882del , CM000673.1:g.113780881_113780882del	GRCh37
NC_000011.8:g.113286091_113286092del	NCBI36
NG_011483.1:g.10293_10294del

Transcript Alleles

HGVS	Amino-acid change
ENST00000260191.8:c.213+704_213+705del MANE Select	ENSP00000260191.2:n.213+704_213+705del
ENST00000260191.7:c.213+704_213+705del	ENSP00000260191.2:n.213+704_213+705del
ENST00000260191.6:c.213+704_213+705del	ENSP00000260191.2:n.213+704_213+705del
ENST00000537778.5:c.180+704_180+705del	ENSP00000443118.1:n.180+704_180+705del
NM_006028.4:c.213+704_213+705del	NP_006019.1:n.213+704_213+705del
XM_011543063.1:c.180+704_180+705del	XP_011541365.1:n.180+704_180+705del
XM_011543064.1:c.12+11076_12+11077del	XP_011541366.1:n.12+11076_12+11077del
XM_011543066.1:c.180+704_180+705del	XP_011541368.1:n.180+704_180+705del
NM_001363563.1:c.180+704_180+705del	NP_001350492.1:n.180+704_180+705del
XM_024448767.1:c.-82+704_-82+705del	XP_024304535.1:n.-82+704_-82+705del
XR_001748034.2:n.464+704_464+705del
NM_001363563.2:c.180+704_180+705del	NP_001350492.1:n.180+704_180+705del
NM_006028.5:c.213+704_213+705del MANE Select	NP_006019.1:n.213+704_213+705del