Canonical Allele Identifier: CA2001379851
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903438T= , CM000673.2:g.113903438T= GRCh38
NC_000011.9:g.113774160T= , CM000673.1:g.113774160T= GRCh37
NC_000011.8:g.113279370T= NCBI36
NG_011483.1:g.3572T=

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4355T= XP_011541366.1:n.12+4355T=
XM_024448767.1:c.-243+4355T= XP_024304535.1:n.-243+4355T=