Canonical Allele Identifier: CA249233039

Gene: HTR2A HTR2A-AS1

Linked Data

• dbSNP Id: rs7984966
• gnomAD v3: 13-46855311-T-A
• gnomAD v4: 13-46855311-T-A
• MyVariant Identifiers: chr13:g.47429446T>A (hg19) ; chr13:g.46855311T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46855311T>A , CM000675.2:g.46855311T>A	GRCh38
NC_000013.10:g.47429446T>A , CM000675.1:g.47429446T>A	GRCh37
NC_000013.9:g.46327447T>A	NCBI36
NG_013011.1:g.46724A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-19672A>T (HTR2A) MANE Select	ENSP00000437737.1:n.614-19672A>T
ENST00000543956.5:c.125-19672A>T (HTR2A)	ENSP00000441861.2:n.125-19672A>T
ENST00000378688.8:c.614-19672A>T (HTR2A)	ENSP00000367959.3:n.614-19672A>T
ENST00000542664.3:c.614-19672A>T (HTR2A)	ENSP00000437737.1:n.614-19672A>T
ENST00000543956.4:c.362-19672A>T (HTR2A)	ENSP00000441861.1:n.362-19672A>T
NM_000621.4:c.614-19672A>T (HTR2A)	NP_000612.1:n.614-19672A>T
NM_001165947.2:c.362-19672A>T (HTR2A)	NP_001159419.1:n.362-19672A>T
NR_046612.1:n.232-779T>A (HTR2A-AS1)
NR_103752.1:n.88-779T>A (HTR2A-AS1)
NM_000621.5:c.614-19672A>T (HTR2A) MANE Select	NP_000612.1:n.614-19672A>T
NM_001165947.5:c.125-19672A>T (HTR2A)	NP_001159419.2:n.125-19672A>T
NM_001378924.1:c.614-19672A>T (HTR2A)	NP_001365853.1:n.614-19672A>T