Canonical Allele Identifier: CA355380043
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183778090C>T (hg19) chr3:g.184060302C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060302C>T , CM000665.2:g.184060302C>T GRCh38
NC_000003.11:g.183778090C>T , CM000665.1:g.183778090C>T GRCh37
NC_000003.10:g.185260784C>T NCBI36
NG_012749.1:g.12256C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1294C>T MANE Select ENSP00000322617.1:p.Leu432Phe
ENST00000318351.1:c.1294C>T ENSP00000322617.1:p.Leu432Phe
NM_130770.2:c.1294C>T NP_570126.2:p.Leu432Phe
NM_130770.3:c.1294C>T MANE Select NP_570126.2:p.Leu432Phe
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