Canonical Allele Identifier: CA366067981

Gene: CCDC170

Linked Data

• dbSNP Id: rs1776953590
• MyVariant Identifiers: chr6:g.151936765T>G (hg19) ; chr6:g.151615630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615630T>G , CM000668.2:g.151615630T>G	GRCh38
NC_000006.11:g.151936765T>G , CM000668.1:g.151936765T>G	GRCh37
NC_000006.10:g.151978458T>G	NCBI36
NG_021198.1:g.126591T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1898T>G MANE Select	ENSP00000239374.6:p.Met633Arg
ENST00000239374.7:c.1898T>G	ENSP00000239374.6:p.Met633Arg
NM_025059.3:c.1898T>G	NP_079335.2:p.Met633Arg
XM_011536147.1:c.1916T>G	XP_011534449.1:p.Met639Arg
XM_011536148.1:c.1715T>G	XP_011534450.1:p.Met572Arg
XM_011536147.2:c.1916T>G	XP_011534449.1:p.Met639Arg
XM_011536148.2:c.1715T>G	XP_011534450.1:p.Met572Arg
XR_001743865.1:n.129+1091A>C
NM_025059.4:c.1898T>G MANE Select	NP_079335.2:p.Met633Arg