Canonical Allele Identifier: CA2001379877
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs1949710324

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903473dup , CM000673.2:g.113903473dup GRCh38
NC_000011.9:g.113774195dup , CM000673.1:g.113774195dup GRCh37
NC_000011.8:g.113279405dup NCBI36
NG_011483.1:g.3607dup

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4390dup XP_011541366.1:n.12+4390dup
XM_024448767.1:c.-243+4390dup XP_024304535.1:n.-243+4390dup