Canonical Allele Identifier: CA2001379821
Gene: HTR3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903414_113903419delinsATTTCT , CM000673.2:g.113903414_113903419delinsATTTCT GRCh38
NC_000011.9:g.113774136_113774141delinsATTTCT , CM000673.1:g.113774136_113774141delinsATTTCT GRCh37
NC_000011.8:g.113279346_113279351delinsATTTCT NCBI36
NG_011483.1:g.3548_3553delinsATTTCT

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4331_12+4336delinsATTTCT XP_011541366.1:n.12+4331_12+4336delinsATTTCT
XM_024448767.1:c.-243+4331_-243+4336delinsATTTCT XP_024304535.1:n.-243+4331_-243+4336delinsATTTCT