Canonical Allele Identifier: CA355379028
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.184060000del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060000del , CM000665.2:g.184060000del GRCh38
NC_000003.11:g.183777788del , CM000665.1:g.183777788del GRCh37
NC_000003.10:g.185260482del NCBI36
NG_012749.1:g.11954del

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1098del MANE Select ENSP00000322617.1:p.Lys367ArgfsTer22
ENST00000318351.1:c.1098del ENSP00000322617.1:p.Lys367ArgfsTer22
NM_130770.2:c.1098del NP_570126.2:p.Lys367ArgfsTer22
NM_130770.3:c.1098del MANE Select NP_570126.2:p.Lys367ArgfsTer22
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Search 100 bp 3'