Canonical Allele Identifier: CA609566026

Gene: HTR2A HTR2A-AS1

Linked Data

• dbSNP Id: rs1398666947
• gnomAD v2: 13-47428608-A-G
• MyVariant Identifiers: chr13:g.47428608A>G (hg19) ; chr13:g.46854473A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46854473A>G , CM000675.2:g.46854473A>G	GRCh38
NC_000013.10:g.47428608A>G , CM000675.1:g.47428608A>G	GRCh37
NC_000013.9:g.46326609A>G	NCBI36
NG_013011.1:g.47562T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-18834T>C (HTR2A) MANE Select	ENSP00000437737.1:n.614-18834T>C
ENST00000543956.5:c.125-18834T>C (HTR2A)	ENSP00000441861.2:n.125-18834T>C
ENST00000378688.8:c.614-18834T>C (HTR2A)	ENSP00000367959.3:n.614-18834T>C
ENST00000542664.3:c.614-18834T>C (HTR2A)	ENSP00000437737.1:n.614-18834T>C
ENST00000543956.4:c.362-18834T>C (HTR2A)	ENSP00000441861.1:n.362-18834T>C
NM_000621.4:c.614-18834T>C (HTR2A)	NP_000612.1:n.614-18834T>C
NM_001165947.2:c.362-18834T>C (HTR2A)	NP_001159419.1:n.362-18834T>C
NR_046612.1:n.231+391A>G (HTR2A-AS1)
NR_103752.1:n.88-1617A>G (HTR2A-AS1)
NM_000621.5:c.614-18834T>C (HTR2A) MANE Select	NP_000612.1:n.614-18834T>C
NM_001165947.5:c.125-18834T>C (HTR2A)	NP_001159419.2:n.125-18834T>C
NM_001378924.1:c.614-18834T>C (HTR2A)	NP_001365853.1:n.614-18834T>C