Canonical Allele Identifier: CA437322706
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1723408924
MyVariant Identifiers: chr3:g.183777653C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059865C>A , CM000665.2:g.184059865C>A GRCh38
NC_000003.11:g.183777653C>A , CM000665.1:g.183777653C>A GRCh37
NC_000003.10:g.185260347C>A NCBI36
NG_012749.1:g.11819C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.963C>A MANE Select ENSP00000322617.1:p.Val321=
ENST00000318351.1:c.963C>A ENSP00000322617.1:p.Val321=
NM_130770.2:c.963C>A NP_570126.2:p.Val321=
NM_130770.3:c.963C>A MANE Select NP_570126.2:p.Val321=
Search 100 bp 5'
Search 100 bp 3'