Canonical Allele Identifier: CA355380131
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1452828121
gnomAD v2: 3-183778111-C-T
gnomAD v4: 3-184060323-C-T
MyVariant Identifiers: chr3:g.183778111C>T (hg19) chr3:g.184060323C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060323C>T , CM000665.2:g.184060323C>T GRCh38
NC_000003.11:g.183778111C>T , CM000665.1:g.183778111C>T GRCh37
NC_000003.10:g.185260805C>T NCBI36
NG_012749.1:g.12277C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1315C>T MANE Select ENSP00000322617.1:p.Leu439Phe
ENST00000318351.1:c.1315C>T ENSP00000322617.1:p.Leu439Phe
NM_130770.2:c.1315C>T NP_570126.2:p.Leu439Phe
NM_130770.3:c.1315C>T MANE Select NP_570126.2:p.Leu439Phe
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Search 100 bp 3'