Canonical Allele Identifier: CA388152993

Gene: HTR2A

Linked Data

• gnomAD v4: 13-46892509-T-C
• MyVariant Identifiers: chr13:g.47466644T>C (hg19) ; chr13:g.46892509T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892509T>C , CM000675.2:g.46892509T>C	GRCh38
NC_000013.10:g.47466644T>C , CM000675.1:g.47466644T>C	GRCh37
NC_000013.9:g.46364645T>C	NCBI36
NG_013011.1:g.9526A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.494A>G MANE Select	ENSP00000437737.1:p.His165Arg
ENST00000543956.5:c.5A>G	ENSP00000441861.2:p.His2Arg
ENST00000378688.8:c.494A>G	ENSP00000367959.3:p.His165Arg
ENST00000542664.3:c.494A>G	ENSP00000437737.1:p.His165Arg
ENST00000543956.4:c.242A>G	ENSP00000441861.1:p.His81Arg
NM_000621.4:c.494A>G	NP_000612.1:p.His165Arg
NM_001165947.2:c.242A>G	NP_001159419.1:p.His81Arg
NM_000621.5:c.494A>G MANE Select	NP_000612.1:p.His165Arg
NM_001165947.5:c.5A>G	NP_001159419.2:p.His2Arg
NM_001378924.1:c.494A>G	NP_001365853.1:p.His165Arg