Canonical Allele Identifier: CA2001379893

Gene: HTR3B

Linked Data

• dbSNP Id: rs1591566847

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113903494A>G , CM000673.2:g.113903494A>G	GRCh38
NC_000011.9:g.113774216A>G , CM000673.1:g.113774216A>G	GRCh37
NC_000011.8:g.113279426A>G	NCBI36
NG_011483.1:g.3628A>G

Transcript Alleles

HGVS	Amino-acid Change
XM_011543064.1:c.12+4411A>G	XP_011541366.1:n.12+4411A>G
XM_024448767.1:c.-243+4411A>G	XP_024304535.1:n.-243+4411A>G