Canonical Allele Identifier: CA437322995
Gene: HTR3C HGNC NCBI

Linked Data

gnomAD v4: 3-184060003-G-A
MyVariant Identifiers: chr3:g.183777791G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060003G>A , CM000665.2:g.184060003G>A GRCh38
NC_000003.11:g.183777791G>A , CM000665.1:g.183777791G>A GRCh37
NC_000003.10:g.185260485G>A NCBI36
NG_012749.1:g.11957G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1101G>A MANE Select ENSP00000322617.1:p.Lys367=
ENST00000318351.1:c.1101G>A ENSP00000322617.1:p.Lys367=
NM_130770.2:c.1101G>A NP_570126.2:p.Lys367=
NM_130770.3:c.1101G>A MANE Select NP_570126.2:p.Lys367=
Search 100 bp 5'
Search 100 bp 3'