Canonical Allele Identifier: CA2001379863

Gene: HTR3B

Linked Data

• dbSNP Id: rs1451993498

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903452C>A , CM000673.2:g.113903452C>A	GRCh38
NC_000011.9:g.113774174C>A , CM000673.1:g.113774174C>A	GRCh37
NC_000011.8:g.113279384C>A	NCBI36
NG_011483.1:g.3586C>A

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4369C>A	XP_011541366.1:n.12+4369C>A
XM_024448767.1:c.-243+4369C>A	XP_024304535.1:n.-243+4369C>A