Canonical Allele Identifier: CA609929193

Gene: HTR2A

Linked Data

• dbSNP Id: rs1329968736
• gnomAD v2: 13-47470073-TAGA-T
• gnomAD v3: 13-46895938-TAGA-T
• gnomAD v4: 13-46895938-TAGA-T
• MyVariant Identifiers: chr13:g.47470074_47470076del (hg19) ; chr13:g.46895939_46895941del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895941_46895943del , CM000675.2:g.46895941_46895943del	GRCh38
NC_000013.10:g.47470076_47470078del , CM000675.1:g.47470076_47470078del	GRCh37
NC_000013.9:g.46368077_46368079del	NCBI36
NG_013011.1:g.6094_6096del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.-35_-33del MANE Select	ENSP00000437737.1:n.-35_-33del
ENST00000543956.5:c.-78+733_-78+735del	ENSP00000441861.2:n.-78+733_-78+735del
ENST00000378688.8:c.-35_-33del	ENSP00000367959.3:n.-35_-33del
ENST00000542664.3:c.-35_-33del	ENSP00000437737.1:n.-35_-33del
ENST00000543956.4:c.160+733_160+735del	ENSP00000441861.1:n.160+733_160+735del
NM_000621.4:c.-35_-33del	NP_000612.1:n.-35_-33del
NM_001165947.2:c.160+733_160+735del	NP_001159419.1:n.160+733_160+735del
NM_000621.5:c.-35_-33del MANE Select	NP_000612.1:n.-35_-33del
NM_001165947.5:c.-78+733_-78+735del	NP_001159419.2:n.-78+733_-78+735del
NM_001378924.1:c.-35_-33del	NP_001365853.1:n.-35_-33del