Canonical Allele Identifier: CA1095909635

Gene: CCDC170

Linked Data

• dbSNP Id: rs1782418088
• gnomAD v3: 6-151526822-C-T
• gnomAD v4: 6-151526822-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151526822C>T , CM000668.2:g.151526822C>T	GRCh38
NC_000006.11:g.151847957C>T , CM000668.1:g.151847957C>T	GRCh37
NC_000006.10:g.151889650C>T	NCBI36
NG_021198.1:g.37783C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.58-9496C>T MANE Select	ENSP00000239374.6:n.58-9496C>T
ENST00000239374.7:c.58-9496C>T	ENSP00000239374.6:n.58-9496C>T
NM_025059.3:c.58-9496C>T	NP_079335.2:n.58-9496C>T
NM_025059.4:c.58-9496C>T MANE Select	NP_079335.2:n.58-9496C>T