Canonical Allele Identifier: CA609569273

Gene: HTR2A

Linked Data

• dbSNP Id: rs1417514261
• gnomAD v2: 13-47466903-A-AGC
• gnomAD v3: 13-46892768-A-AGC
• gnomAD v4: 13-46892768-A-AGC
• MyVariant Identifiers: chr13:g.47466903_47466904insGC (hg19) ; chr13:g.46892768_46892769insGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892769_46892770dup , CM000675.2:g.46892769_46892770dup	GRCh38
NC_000013.10:g.47466904_47466905dup , CM000675.1:g.47466904_47466905dup	GRCh37
NC_000013.9:g.46364905_46364906dup	NCBI36
NG_013011.1:g.9265_9266dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413-180_413-179dup MANE Select	ENSP00000437737.1:n.413-180_413-179dup
ENST00000543956.5:c.-77-180_-77-179dup	ENSP00000441861.2:n.-77-180_-77-179dup
ENST00000378688.8:c.413-180_413-179dup	ENSP00000367959.3:n.413-180_413-179dup
ENST00000542664.3:c.413-180_413-179dup	ENSP00000437737.1:n.413-180_413-179dup
ENST00000543956.4:c.161-180_161-179dup	ENSP00000441861.1:n.161-180_161-179dup
NM_000621.4:c.413-180_413-179dup	NP_000612.1:n.413-180_413-179dup
NM_001165947.2:c.161-180_161-179dup	NP_001159419.1:n.161-180_161-179dup
NM_000621.5:c.413-180_413-179dup MANE Select	NP_000612.1:n.413-180_413-179dup
NM_001165947.5:c.-77-180_-77-179dup	NP_001159419.2:n.-77-180_-77-179dup
NM_001378924.1:c.413-180_413-179dup	NP_001365853.1:n.413-180_413-179dup