Canonical Allele Identifier: CA2089311802

Gene: HTR2A

Linked Data

• dbSNP Id: rs1951101910

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46896067_46896070del , CM000675.2:g.46896067_46896070del	GRCh38
NC_000013.10:g.47470202_47470205del , CM000675.1:g.47470202_47470205del	GRCh37
NC_000013.9:g.46368203_46368206del	NCBI36
NG_013011.1:g.5967_5970del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-162_-159del MANE Select	ENSP00000437737.1:n.-162_-159del
ENST00000543956.5:c.-78+606_-78+609del	ENSP00000441861.2:n.-78+606_-78+609del
ENST00000542664.3:c.-162_-159del	ENSP00000437737.1:n.-162_-159del
ENST00000543956.4:c.160+606_160+609del	ENSP00000441861.1:n.160+606_160+609del
NM_000621.4:c.-162_-159del	NP_000612.1:n.-162_-159del
NM_001165947.2:c.160+606_160+609del	NP_001159419.1:n.160+606_160+609del
NM_000621.5:c.-162_-159del MANE Select	NP_000612.1:n.-162_-159del
NM_001165947.5:c.-78+606_-78+609del	NP_001159419.2:n.-78+606_-78+609del
NM_001378924.1:c.-162_-159del	NP_001365853.1:n.-162_-159del