Canonical Allele Identifier: CA483555443

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47469955A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895820A>G , CM000675.2:g.46895820A>G	GRCh38
NC_000013.10:g.47469955A>G , CM000675.1:g.47469955A>G	GRCh37
NC_000013.9:g.46367956A>G	NCBI36
NG_013011.1:g.6215T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.87T>C MANE Select	ENSP00000437737.1:p.Ser29=
ENST00000543956.5:c.-78+854T>C	ENSP00000441861.2:n.-78+854T>C
ENST00000378688.8:c.87T>C	ENSP00000367959.3:p.Ser29=
ENST00000542664.3:c.87T>C	ENSP00000437737.1:p.Ser29=
ENST00000543956.4:c.160+854T>C	ENSP00000441861.1:n.160+854T>C
NM_000621.4:c.87T>C	NP_000612.1:p.Ser29=
NM_001165947.2:c.160+854T>C	NP_001159419.1:n.160+854T>C
NM_000621.5:c.87T>C MANE Select	NP_000612.1:p.Ser29=
NM_001165947.5:c.-78+854T>C	NP_001159419.2:n.-78+854T>C
NM_001378924.1:c.87T>C	NP_001365853.1:p.Ser29=