Canonical Allele Identifier: CA2001379872
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903466G= , CM000673.2:g.113903466G= GRCh38
NC_000011.9:g.113774188G= , CM000673.1:g.113774188G= GRCh37
NC_000011.8:g.113279398G= NCBI36
NG_011483.1:g.3600G=

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4383G= XP_011541366.1:n.12+4383G=
XM_024448767.1:c.-243+4383G= XP_024304535.1:n.-243+4383G=