Canonical Allele Identifier: CA483555219

Gene: HTR2A

Linked Data

• MyVariant Identifiers: chr13:g.47469739T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46895604T>G , CM000675.2:g.46895604T>G	GRCh38
NC_000013.10:g.47469739T>G , CM000675.1:g.47469739T>G	GRCh37
NC_000013.9:g.46367740T>G	NCBI36
NG_013011.1:g.6431A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.303A>C MANE Select	ENSP00000437737.1:p.Leu101=
ENST00000543956.5:c.-78+1070A>C	ENSP00000441861.2:n.-78+1070A>C
ENST00000378688.8:c.303A>C	ENSP00000367959.3:p.Leu101=
ENST00000542664.3:c.303A>C	ENSP00000437737.1:p.Leu101=
ENST00000543956.4:c.160+1070A>C	ENSP00000441861.1:n.160+1070A>C
ENST00000612998.1:c.210A>C	ENSP00000482708.1:p.Leu70=
NM_000621.4:c.303A>C	NP_000612.1:p.Leu101=
NM_001165947.2:c.160+1070A>C	NP_001159419.1:n.160+1070A>C
NM_000621.5:c.303A>C MANE Select	NP_000612.1:p.Leu101=
NM_001165947.5:c.-78+1070A>C	NP_001159419.2:n.-78+1070A>C
NM_001378924.1:c.303A>C	NP_001365853.1:p.Leu101=