Canonical Allele Identifier: CA355379524
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183778022C>A (hg19) chr3:g.184060234C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060234C>A , CM000665.2:g.184060234C>A GRCh38
NC_000003.11:g.183778022C>A , CM000665.1:g.183778022C>A GRCh37
NC_000003.10:g.185260716C>A NCBI36
NG_012749.1:g.12188C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1226C>A MANE Select ENSP00000322617.1:p.Thr409Asn
ENST00000318351.1:c.1226C>A ENSP00000322617.1:p.Thr409Asn
NM_130770.2:c.1226C>A NP_570126.2:p.Thr409Asn
NM_130770.3:c.1226C>A MANE Select NP_570126.2:p.Thr409Asn
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