Canonical Allele Identifier: CA355372043
Gene: HTR3C HGNC NCBI

Linked Data

gnomAD v4: 3-184056978-G-C
MyVariant Identifiers: chr3:g.183774766G>C (hg19) chr3:g.184056978G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184056978G>C , CM000665.2:g.184056978G>C GRCh38
NC_000003.11:g.183774766G>C , CM000665.1:g.183774766G>C GRCh37
NC_000003.10:g.185257460G>C NCBI36
NG_012749.1:g.8932G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.493G>C MANE Select ENSP00000322617.1:p.Asp165His
ENST00000318351.1:c.493G>C ENSP00000322617.1:p.Asp165His
NM_130770.2:c.493G>C NP_570126.2:p.Asp165His
NM_130770.3:c.493G>C MANE Select NP_570126.2:p.Asp165His
Search 100 bp 5'
Search 100 bp 3'