Canonical Allele Identifier: CA12213291
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs1038304

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151612040A>G , CM000668.2:g.151612040A>G GRCh38
NC_000006.11:g.151933175A>G , CM000668.1:g.151933175A>G GRCh37
NC_000006.10:g.151974868A>G NCBI36
NG_021198.1:g.123001A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000239374.7:c.1711-3403A>G ENSP00000239374.6:p.=
NM_025059.3:c.1711-3403A>G NP_079335.2:p.=
XM_011536147.1:c.1729-3403A>G XP_011534449.1:p.=
XM_011536148.1:c.1528-3403A>G XP_011534450.1:p.=
XM_011536147.2:c.1729-3403A>G XP_011534449.1:p.=
XM_011536148.2:c.1528-3403A>G XP_011534450.1:p.=
NM_025059.4:c.1711-3403A>G MANE Select NP_079335.2:p.=