Canonical Allele Identifier: CA88819714
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1012423940
MyVariant Identifiers: chr3:g.183777826T>A (hg19) chr3:g.184060038T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060038T>A , CM000665.2:g.184060038T>A GRCh38
NC_000003.11:g.183777826T>A , CM000665.1:g.183777826T>A GRCh37
NC_000003.10:g.185260520T>A NCBI36
NG_012749.1:g.11992T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000318351.2:c.1136T>A MANE Select ENSP00000322617.1:p.Leu379Gln
ENST00000318351.1:c.1136T>A ENSP00000322617.1:p.Leu379Gln
NM_130770.2:c.1136T>A NP_570126.2:p.Leu379Gln
NM_130770.3:c.1136T>A MANE Select NP_570126.2:p.Leu379Gln
Search 100 bp 5'
Search 100 bp 3'