Canonical Allele Identifier: CA150156360

Gene: CCDC170

Linked Data

• dbSNP Id: rs74568352
• gnomAD v4: 6-151618628-C-T
• MyVariant Identifiers: chr6:g.151939763C>T (hg19) ; chr6:g.151618628C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618628C>T , CM000668.2:g.151618628C>T	GRCh38
NC_000006.11:g.151939763C>T , CM000668.1:g.151939763C>T	GRCh37
NC_000006.10:g.151981456C>T	NCBI36
NG_021198.1:g.129589C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*481C>T MANE Select	ENSP00000239374.6:n.*481C>T
ENST00000239374.7:c.*481C>T	ENSP00000239374.6:n.*481C>T
NM_025059.3:c.*481C>T	NP_079335.2:n.*481C>T
XM_011536147.1:c.*481C>T	XP_011534449.1:n.*481C>T
XM_011536148.1:c.*481C>T	XP_011534450.1:n.*481C>T
XM_011536147.2:c.*481C>T	XP_011534449.1:n.*481C>T
XM_011536148.2:c.*481C>T	XP_011534450.1:n.*481C>T
NM_025059.4:c.*481C>T MANE Select	NP_079335.2:n.*481C>T