Canonical Allele Identifier: CA355379535
Gene: HTR3C HGNC NCBI

Linked Data

dbSNP Id: rs1723419484
MyVariant Identifiers: chr3:g.183778027C>G (hg19) chr3:g.184060239C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060239C>G , CM000665.2:g.184060239C>G GRCh38
NC_000003.11:g.183778027C>G , CM000665.1:g.183778027C>G GRCh37
NC_000003.10:g.185260721C>G NCBI36
NG_012749.1:g.12193C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1231C>G MANE Select ENSP00000322617.1:p.Leu411Val
ENST00000318351.1:c.1231C>G ENSP00000322617.1:p.Leu411Val
NM_130770.2:c.1231C>G NP_570126.2:p.Leu411Val
NM_130770.3:c.1231C>G MANE Select NP_570126.2:p.Leu411Val
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