Canonical Allele Identifier: CA437323002
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777797T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060009T>C , CM000665.2:g.184060009T>C GRCh38
NC_000003.11:g.183777797T>C , CM000665.1:g.183777797T>C GRCh37
NC_000003.10:g.185260491T>C NCBI36
NG_012749.1:g.11963T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1107T>C MANE Select ENSP00000322617.1:p.Asn369=
ENST00000318351.1:c.1107T>C ENSP00000322617.1:p.Asn369=
NM_130770.2:c.1107T>C NP_570126.2:p.Asn369=
NM_130770.3:c.1107T>C MANE Select NP_570126.2:p.Asn369=
Search 100 bp 5'
Search 100 bp 3'