Canonical Allele Identifier: CA2001379829
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903423_113903429delinsCTTTTCT , CM000673.2:g.113903423_113903429delinsCTTTTCT GRCh38
NC_000011.9:g.113774145_113774151delinsCTTTTCT , CM000673.1:g.113774145_113774151delinsCTTTTCT GRCh37
NC_000011.8:g.113279355_113279361delinsCTTTTCT NCBI36
NG_011483.1:g.3557_3563delinsCTTTTCT

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4340_12+4346delinsCTTTTCT XP_011541366.1:n.12+4340_12+4346delinsCTTTTCT
XM_024448767.1:c.-243+4340_-243+4346delinsCTTTTCT XP_024304535.1:n.-243+4340_-243+4346delinsCTTTTCT