Canonical Allele Identifier: CA228695477

Gene: HTR3B

Linked Data

• dbSNP Id: rs950663513
• gnomAD v3: 11-113903287-G-A
• gnomAD v4: 11-113903287-G-A
• MyVariant Identifiers: chr11:g.113774009G>A (hg19) ; chr11:g.113903287G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903287G>A , CM000673.2:g.113903287G>A	GRCh38
NC_000011.9:g.113774009G>A , CM000673.1:g.113774009G>A	GRCh37
NC_000011.8:g.113279219G>A	NCBI36
NG_011483.1:g.3421G>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4204G>A	XP_011541366.1:n.12+4204G>A
XM_024448767.1:c.-243+4204G>A	XP_024304535.1:n.-243+4204G>A