Canonical Allele Identifier: CA388153746

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47469768T>G (hg19) ; chr13:g.46895633T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895633T>G , CM000675.2:g.46895633T>G	GRCh38
NC_000013.10:g.47469768T>G , CM000675.1:g.47469768T>G	GRCh37
NC_000013.9:g.46367769T>G	NCBI36
NG_013011.1:g.6402A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.274A>C MANE Select	ENSP00000437737.1:p.Asn92His
ENST00000543956.5:c.-78+1041A>C	ENSP00000441861.2:n.-78+1041A>C
ENST00000378688.8:c.274A>C	ENSP00000367959.3:p.Asn92His
ENST00000542664.3:c.274A>C	ENSP00000437737.1:p.Asn92His
ENST00000543956.4:c.160+1041A>C	ENSP00000441861.1:n.160+1041A>C
ENST00000612998.1:c.181A>C	ENSP00000482708.1:p.Asn61His
NM_000621.4:c.274A>C	NP_000612.1:p.Asn92His
NM_001165947.2:c.160+1041A>C	NP_001159419.1:n.160+1041A>C
NM_000621.5:c.274A>C MANE Select	NP_000612.1:p.Asn92His
NM_001165947.5:c.-78+1041A>C	NP_001159419.2:n.-78+1041A>C
NM_001378924.1:c.274A>C	NP_001365853.1:p.Asn92His