Canonical Allele Identifier: CA2725778
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs752853537
ExAC: 3:183778033 G / GGGACAAAGACCC
gnomAD v2: 3-183778033-G-GGGACAAAGACCC
gnomAD v4: 3-184060245-G-GGGACAAAGACCC
MyVariant Identifiers: chr3:g.183778033_183778034insGGACAAAGACCC (hg19) chr3:g.184060245_184060246insGGACAAAGACCC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060245_184060246insGGACAAAGACCC , CM000665.2:g.184060245_184060246insGGACAAAGACCC GRCh38
NC_000003.11:g.183778033_183778034insGGACAAAGACCC , CM000665.1:g.183778033_183778034insGGACAAAGACCC GRCh37
NC_000003.10:g.185260727_185260728insGGACAAAGACCC NCBI36
NG_012749.1:g.12199_12200insGGACAAAGACCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1237_1238insGGACAAAGACCC MANE Select ENSP00000322617.1:p.Glu413delinsGlyThrLysThrGln
ENST00000318351.1:c.1237_1238insGGACAAAGACCC ENSP00000322617.1:p.Glu413delinsGlyThrLysThrGln
NM_130770.2:c.1237_1238insGGACAAAGACCC NP_570126.2:p.Glu413delinsGlyThrLysThrGln
NM_130770.3:c.1237_1238insGGACAAAGACCC MANE Select NP_570126.2:p.Glu413delinsGlyThrLysThrGln
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