Canonical Allele Identifier: CA4052038
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs762737537
ExAC: 6:151939261 C / T
gnomAD v2: 6-151939261-C-T
COSMIC: COSM3621507
MyVariant Identifiers: chr6:g.151939261C>T (hg19) chr6:g.151618126C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618126C>T , CM000668.2:g.151618126C>T GRCh38
NC_000006.11:g.151939261C>T , CM000668.1:g.151939261C>T GRCh37
NC_000006.10:g.151980954C>T NCBI36
NG_021198.1:g.129087C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.2127C>T MANE Select ENSP00000239374.6:p.Gly709=
ENST00000239374.7:c.2127C>T ENSP00000239374.6:p.Gly709=
NM_025059.3:c.2127C>T NP_079335.2:p.Gly709=
XM_011536147.1:c.2145C>T XP_011534449.1:p.Gly715=
XM_011536148.1:c.1944C>T XP_011534450.1:p.Gly648=
XM_011536147.2:c.2145C>T XP_011534449.1:p.Gly715=
XM_011536148.2:c.1944C>T XP_011534450.1:p.Gly648=
NM_025059.4:c.2127C>T MANE Select NP_079335.2:p.Gly709=
Search 100 bp 5'
Search 100 bp 3'