Canonical Allele Identifier: CA150155267

Gene: CCDC170

Linked Data

• dbSNP Id: rs537414499
• gnomAD v3: 6-151615451-T-C
• gnomAD v4: 6-151615451-T-C
• MyVariant Identifiers: chr6:g.151936586T>C (hg19) ; chr6:g.151615451T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615451T>C , CM000668.2:g.151615451T>C	GRCh38
NC_000006.11:g.151936586T>C , CM000668.1:g.151936586T>C	GRCh37
NC_000006.10:g.151978279T>C	NCBI36
NG_021198.1:g.126412T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1719T>C MANE Select	ENSP00000239374.6:p.Thr573=
ENST00000239374.7:c.1719T>C	ENSP00000239374.6:p.Thr573=
ENST00000537358.1:n.505T>C
NM_025059.3:c.1719T>C	NP_079335.2:p.Thr573=
XM_011536147.1:c.1737T>C	XP_011534449.1:p.Thr579=
XM_011536148.1:c.1536T>C	XP_011534450.1:p.Thr512=
XM_011536147.2:c.1737T>C	XP_011534449.1:p.Thr579=
XM_011536148.2:c.1536T>C	XP_011534450.1:p.Thr512=
XR_001743865.1:n.129+1270A>G
NM_025059.4:c.1719T>C MANE Select	NP_079335.2:p.Thr573=