Canonical Allele Identifier: CA355379426
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777974T>C (hg19) chr3:g.184060186T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060186T>C , CM000665.2:g.184060186T>C GRCh38
NC_000003.11:g.183777974T>C , CM000665.1:g.183777974T>C GRCh37
NC_000003.10:g.185260668T>C NCBI36
NG_012749.1:g.12140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1178T>C MANE Select ENSP00000322617.1:p.Leu393Pro
ENST00000318351.1:c.1178T>C ENSP00000322617.1:p.Leu393Pro
NM_130770.2:c.1178T>C NP_570126.2:p.Leu393Pro
NM_130770.3:c.1178T>C MANE Select NP_570126.2:p.Leu393Pro
Search 100 bp 5'
Search 100 bp 3'