Canonical Allele Identifier: CA355378965
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777777A>G (hg19) chr3:g.184059989A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059989A>G , CM000665.2:g.184059989A>G GRCh38
NC_000003.11:g.183777777A>G , CM000665.1:g.183777777A>G GRCh37
NC_000003.10:g.185260471A>G NCBI36
NG_012749.1:g.11943A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1087A>G MANE Select ENSP00000322617.1:p.Thr363Ala
ENST00000318351.1:c.1087A>G ENSP00000322617.1:p.Thr363Ala
NM_130770.2:c.1087A>G NP_570126.2:p.Thr363Ala
NM_130770.3:c.1087A>G MANE Select NP_570126.2:p.Thr363Ala
Search 100 bp 5'
Search 100 bp 3'