Canonical Allele Identifier: CA6977479

Gene: HTR2A

Linked Data

• dbSNP Id: rs755032042
• ExAC: 13:47408942 C / A
• gnomAD v2: 13-47408942-C-A
• gnomAD v4: 13-46834807-C-A
• MyVariant Identifiers: chr13:g.47408942C>A (hg19) ; chr13:g.46834807C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46834807C>A , CM000675.2:g.46834807C>A	GRCh38
NC_000013.10:g.47408942C>A , CM000675.1:g.47408942C>A	GRCh37
NC_000013.9:g.46306943C>A	NCBI36
NG_013011.1:g.67228G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.*30G>T MANE Select	ENSP00000437737.1:n.*30G>T
ENST00000543956.5:c.*30G>T	ENSP00000441861.2:n.*30G>T
ENST00000378688.8:c.*30G>T	ENSP00000367959.3:n.*30G>T
ENST00000542664.3:c.*30G>T	ENSP00000437737.1:n.*30G>T
ENST00000543956.4:c.*30G>T	ENSP00000441861.1:n.*30G>T
NM_000621.4:c.*30G>T	NP_000612.1:n.*30G>T
NM_001165947.2:c.*30G>T	NP_001159419.1:n.*30G>T
NM_000621.5:c.*30G>T MANE Select	NP_000612.1:n.*30G>T
NM_001165947.5:c.*30G>T	NP_001159419.2:n.*30G>T
NM_001378924.1:c.*30G>T	NP_001365853.1:n.*30G>T