Canonical Allele Identifier: CA2001379868
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903461_113903465delinsCCTCT , CM000673.2:g.113903461_113903465delinsCCTCT GRCh38
NC_000011.9:g.113774183_113774187delinsCCTCT , CM000673.1:g.113774183_113774187delinsCCTCT GRCh37
NC_000011.8:g.113279393_113279397delinsCCTCT NCBI36
NG_011483.1:g.3595_3599delinsCCTCT

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4378_12+4382delinsCCTCT XP_011541366.1:n.12+4378_12+4382delinsCCTCT
XM_024448767.1:c.-243+4378_-243+4382delinsCCTCT XP_024304535.1:n.-243+4378_-243+4382delinsCCTCT