Canonical Allele Identifier: CA13844399
Gene: HTR2A HGNC NCBI
HTR2A-AS1 HGNC NCBI
COSMIC:
COSN6626125 (not active)
MyVariant.info:
GRCh38 chr13:g.46855311T>C
GRCh37 chr13:g.47429446T>C
gnomAD v2:
13:47429446 T / C
gnomAD v3:
13:46855311 T / C
gnomAD v4:
chr13-46855311-T-C
Joint Max Group AF 0.34360565 (AFR)
Genomes Max Group AF 0.34360565 (AFR)
dbSNP:
7984966
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Genomic Alleles

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

Transcript Alleles

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