Canonical Allele Identifier: CA249226970

Gene: HTR2A

Linked Data

• dbSNP Id: rs747807657
• gnomAD v2: 13-47423623-G-A
• gnomAD v3: 13-46849488-G-A
• gnomAD v4: 13-46849488-G-A
• MyVariant Identifiers: chr13:g.47423623G>A (hg19) ; chr13:g.46849488G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46849488G>A , CM000675.2:g.46849488G>A	GRCh38
NC_000013.10:g.47423623G>A , CM000675.1:g.47423623G>A	GRCh37
NC_000013.9:g.46321624G>A	NCBI36
NG_013011.1:g.52547C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000542664.4:c.614-13849C>T MANE Select	ENSP00000437737.1:n.614-13849C>T
ENST00000543956.5:c.125-13849C>T	ENSP00000441861.2:n.125-13849C>T
ENST00000378688.8:c.614-13849C>T	ENSP00000367959.3:n.614-13849C>T
ENST00000542664.3:c.614-13849C>T	ENSP00000437737.1:n.614-13849C>T
ENST00000543956.4:c.362-13849C>T	ENSP00000441861.1:n.362-13849C>T
NM_000621.4:c.614-13849C>T	NP_000612.1:n.614-13849C>T
NM_001165947.2:c.362-13849C>T	NP_001159419.1:n.362-13849C>T
NM_000621.5:c.614-13849C>T MANE Select	NP_000612.1:n.614-13849C>T
NM_001165947.5:c.125-13849C>T	NP_001159419.2:n.125-13849C>T
NM_001378924.1:c.614-13849C>T	NP_001365853.1:n.614-13849C>T