Canonical Allele Identifier: CA2001379840
Gene: HTR3B HGNC NCBI

Linked Data

dbSNP Id: rs57289369
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113903436_113903447del , CM000673.2:g.113903436_113903447del GRCh38
NC_000011.9:g.113774158_113774169del , CM000673.1:g.113774158_113774169del GRCh37
NC_000011.8:g.113279368_113279379del NCBI36
NG_011483.1:g.3570_3581del

Transcript Alleles

HGVS Amino-acid Change
XM_011543064.1:c.12+4353_12+4364del XP_011541366.1:n.12+4353_12+4364del
XM_024448767.1:c.-243+4353_-243+4364del XP_024304535.1:n.-243+4353_-243+4364del
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