Canonical Allele Identifier: CA437322986
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183777785C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184059997C>G , CM000665.2:g.184059997C>G GRCh38
NC_000003.11:g.183777785C>G , CM000665.1:g.183777785C>G GRCh37
NC_000003.10:g.185260479C>G NCBI36
NG_012749.1:g.11951C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1095C>G MANE Select ENSP00000322617.1:p.Pro365=
ENST00000318351.1:c.1095C>G ENSP00000322617.1:p.Pro365=
NM_130770.2:c.1095C>G NP_570126.2:p.Pro365=
NM_130770.3:c.1095C>G MANE Select NP_570126.2:p.Pro365=
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