Canonical Allele Identifier: CA366067848

Gene: CCDC170

Linked Data

• dbSNP Id: rs1776953010
• gnomAD v4: 6-151615609-T-C
• MyVariant Identifiers: chr6:g.151936744T>C (hg19) ; chr6:g.151615609T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615609T>C , CM000668.2:g.151615609T>C	GRCh38
NC_000006.11:g.151936744T>C , CM000668.1:g.151936744T>C	GRCh37
NC_000006.10:g.151978437T>C	NCBI36
NG_021198.1:g.126570T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1877T>C MANE Select	ENSP00000239374.6:p.Ile626Thr
ENST00000239374.7:c.1877T>C	ENSP00000239374.6:p.Ile626Thr
NM_025059.3:c.1877T>C	NP_079335.2:p.Ile626Thr
XM_011536147.1:c.1895T>C	XP_011534449.1:p.Ile632Thr
XM_011536148.1:c.1694T>C	XP_011534450.1:p.Ile565Thr
XM_011536147.2:c.1895T>C	XP_011534449.1:p.Ile632Thr
XM_011536148.2:c.1694T>C	XP_011534450.1:p.Ile565Thr
XR_001743865.1:n.129+1112A>G
NM_025059.4:c.1877T>C MANE Select	NP_079335.2:p.Ile626Thr