Canonical Allele Identifier: CA452745915

Gene: CCDC170

Linked Data

• dbSNP Id: rs1776999370
• gnomAD v3: 6-151618123-A-G
• gnomAD v4: 6-151618123-A-G
• MyVariant Identifiers: chr6:g.151939258A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618123A>G , CM000668.2:g.151618123A>G	GRCh38
NC_000006.11:g.151939258A>G , CM000668.1:g.151939258A>G	GRCh37
NC_000006.10:g.151980951A>G	NCBI36
NG_021198.1:g.129084A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.2124A>G MANE Select	ENSP00000239374.6:p.Gln708=
ENST00000239374.7:c.2124A>G	ENSP00000239374.6:p.Gln708=
NM_025059.3:c.2124A>G	NP_079335.2:p.Gln708=
XM_011536147.1:c.2142A>G	XP_011534449.1:p.Gln714=
XM_011536148.1:c.1941A>G	XP_011534450.1:p.Gln647=
XM_011536147.2:c.2142A>G	XP_011534449.1:p.Gln714=
XM_011536148.2:c.1941A>G	XP_011534450.1:p.Gln647=
NM_025059.4:c.2124A>G MANE Select	NP_079335.2:p.Gln708=