Canonical Allele Identifier: CA609929156

Gene: HTR2A

Linked Data

• dbSNP Id: rs397947348
• gnomAD v2: 13-47408913-T-TC
• gnomAD v3: 13-46834778-T-TC
• gnomAD v4: 13-46834778-T-TC
• MyVariant Identifiers: chr13:g.47408913_47408914insC (hg19) ; chr13:g.46834778_46834779insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834780dup , CM000675.2:g.46834780dup	GRCh38
NC_000013.10:g.47408915dup , CM000675.1:g.47408915dup	GRCh37
NC_000013.9:g.46306916dup	NCBI36
NG_013011.1:g.67256dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.*58dup MANE Select	ENSP00000437737.1:n.*58dup
ENST00000543956.5:c.*58dup	ENSP00000441861.2:n.*58dup
ENST00000378688.8:c.*58dup	ENSP00000367959.3:n.*58dup
ENST00000542664.3:c.*58dup	ENSP00000437737.1:n.*58dup
ENST00000543956.4:c.*58dup	ENSP00000441861.1:n.*58dup
NM_000621.4:c.*58dup	NP_000612.1:n.*58dup
NM_001165947.2:c.*58dup	NP_001159419.1:n.*58dup
NM_000621.5:c.*58dup MANE Select	NP_000612.1:n.*58dup
NM_001165947.5:c.*58dup	NP_001159419.2:n.*58dup
NM_001378924.1:c.*58dup	NP_001365853.1:n.*58dup