Canonical Allele Identifier: CA609929180

Gene: HTR2A

Linked Data

• dbSNP Id: rs1318730375
• gnomAD v2: 13-47466741-T-C
• gnomAD v4: 13-46892606-T-C
• MyVariant Identifiers: chr13:g.47466741T>C (hg19) ; chr13:g.46892606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892606T>C , CM000675.2:g.46892606T>C	GRCh38
NC_000013.10:g.47466741T>C , CM000675.1:g.47466741T>C	GRCh37
NC_000013.9:g.46364742T>C	NCBI36
NG_013011.1:g.9429A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413-16A>G MANE Select	ENSP00000437737.1:n.413-16A>G
ENST00000543956.5:c.-77-16A>G	ENSP00000441861.2:n.-77-16A>G
ENST00000378688.8:c.413-16A>G	ENSP00000367959.3:n.413-16A>G
ENST00000542664.3:c.413-16A>G	ENSP00000437737.1:n.413-16A>G
ENST00000543956.4:c.161-16A>G	ENSP00000441861.1:n.161-16A>G
NM_000621.4:c.413-16A>G	NP_000612.1:n.413-16A>G
NM_001165947.2:c.161-16A>G	NP_001159419.1:n.161-16A>G
NM_000621.5:c.413-16A>G MANE Select	NP_000612.1:n.413-16A>G
NM_001165947.5:c.-77-16A>G	NP_001159419.2:n.-77-16A>G
NM_001378924.1:c.413-16A>G	NP_001365853.1:n.413-16A>G