Canonical Allele Identifier: CA355372038
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183774764T>G (hg19) chr3:g.184056976T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184056976T>G , CM000665.2:g.184056976T>G GRCh38
NC_000003.11:g.183774764T>G , CM000665.1:g.183774764T>G GRCh37
NC_000003.10:g.185257458T>G NCBI36
NG_012749.1:g.8930T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.491T>G MANE Select ENSP00000322617.1:p.Leu164Arg
ENST00000318351.1:c.491T>G ENSP00000322617.1:p.Leu164Arg
NM_130770.2:c.491T>G NP_570126.2:p.Leu164Arg
NM_130770.3:c.491T>G MANE Select NP_570126.2:p.Leu164Arg
Search 100 bp 5'
Search 100 bp 3'