Canonical Allele Identifier: CA388150869

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46835040-G-C
• MyVariant Identifiers: chr13:g.47409175G>C (hg19) ; chr13:g.46835040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46835040G>C , CM000675.2:g.46835040G>C	GRCh38
NC_000013.10:g.47409175G>C , CM000675.1:g.47409175G>C	GRCh37
NC_000013.9:g.46307176G>C	NCBI36
NG_013011.1:g.66995C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.1213C>G MANE Select	ENSP00000437737.1:p.Pro405Ala
ENST00000543956.5:c.724C>G	ENSP00000441861.2:p.Pro242Ala
ENST00000378688.8:c.1213C>G	ENSP00000367959.3:p.Pro405Ala
ENST00000542664.3:c.1213C>G	ENSP00000437737.1:p.Pro405Ala
ENST00000543956.4:c.961C>G	ENSP00000441861.1:p.Pro321Ala
NM_000621.4:c.1213C>G	NP_000612.1:p.Pro405Ala
NM_001165947.2:c.961C>G	NP_001159419.1:p.Pro321Ala
NM_000621.5:c.1213C>G MANE Select	NP_000612.1:p.Pro405Ala
NM_001165947.5:c.724C>G	NP_001159419.2:p.Pro242Ala
NM_001378924.1:c.1213C>G	NP_001365853.1:p.Pro405Ala