Canonical Allele Identifier: CA150156281

Gene: CCDC170

Linked Data

• dbSNP Id: rs530442293
• gnomAD v3: 6-151618336-G-T
• gnomAD v4: 6-151618336-G-T
• MyVariant Identifiers: chr6:g.151939471G>T (hg19) ; chr6:g.151618336G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618336G>T , CM000668.2:g.151618336G>T	GRCh38
NC_000006.11:g.151939471G>T , CM000668.1:g.151939471G>T	GRCh37
NC_000006.10:g.151981164G>T	NCBI36
NG_021198.1:g.129297G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*189G>T MANE Select	ENSP00000239374.6:n.*189G>T
ENST00000239374.7:c.*189G>T	ENSP00000239374.6:n.*189G>T
NM_025059.3:c.*189G>T	NP_079335.2:n.*189G>T
XM_011536147.1:c.*189G>T	XP_011534449.1:n.*189G>T
XM_011536148.1:c.*189G>T	XP_011534450.1:n.*189G>T
XM_011536147.2:c.*189G>T	XP_011534449.1:n.*189G>T
XM_011536148.2:c.*189G>T	XP_011534450.1:n.*189G>T
NM_025059.4:c.*189G>T MANE Select	NP_079335.2:n.*189G>T