Canonical Allele Identifier: CA548793713
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1411584660
gnomAD v2: 3-183777999-T-TGGGG
gnomAD v3: 3-184060211-T-TGGGG
gnomAD v4: 3-184060211-T-TGGGG
MyVariant Identifiers: chr3:g.183777999_183778000insGGGG (hg19) chr3:g.184060211_184060212insGGGG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060213_184060216dup , CM000665.2:g.184060213_184060216dup GRCh38
NC_000003.11:g.183778001_183778004dup , CM000665.1:g.183778001_183778004dup GRCh37
NC_000003.10:g.185260695_185260698dup NCBI36
NG_012749.1:g.12167_12170dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1205_1208dup MANE Select ENSP00000322617.1:p.Ser404GlyfsTer?
ENST00000318351.1:c.1205_1208dup ENSP00000322617.1:p.Ser404GlyfsTer?
NM_130770.2:c.1205_1208dup NP_570126.2:p.Ser404GlyfsTer?
NM_130770.3:c.1205_1208dup MANE Select NP_570126.2:p.Ser404GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'