Canonical Allele Identifier: CA355379540
Gene: HTR3C HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.183778030A>C (hg19) chr3:g.184060242A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184060242A>C , CM000665.2:g.184060242A>C GRCh38
NC_000003.11:g.183778030A>C , CM000665.1:g.183778030A>C GRCh37
NC_000003.10:g.185260724A>C NCBI36
NG_012749.1:g.12196A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318351.2:c.1234A>C MANE Select ENSP00000322617.1:p.Met412Leu
ENST00000318351.1:c.1234A>C ENSP00000322617.1:p.Met412Leu
NM_130770.2:c.1234A>C NP_570126.2:p.Met412Leu
NM_130770.3:c.1234A>C MANE Select NP_570126.2:p.Met412Leu
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