Canonical Allele Identifier: CA366067922
Gene: CCDC170 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.151936759G>C (hg19) chr6:g.151615624G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615624G>C , CM000668.2:g.151615624G>C GRCh38
NC_000006.11:g.151936759G>C , CM000668.1:g.151936759G>C GRCh37
NC_000006.10:g.151978452G>C NCBI36
NG_021198.1:g.126585G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1892G>C MANE Select ENSP00000239374.6:p.Ser631Thr
ENST00000239374.7:c.1892G>C ENSP00000239374.6:p.Ser631Thr
NM_025059.3:c.1892G>C NP_079335.2:p.Ser631Thr
XM_011536147.1:c.1910G>C XP_011534449.1:p.Ser637Thr
XM_011536148.1:c.1709G>C XP_011534450.1:p.Ser570Thr
XM_011536147.2:c.1910G>C XP_011534449.1:p.Ser637Thr
XM_011536148.2:c.1709G>C XP_011534450.1:p.Ser570Thr
XR_001743865.1:n.129+1097C>G
NM_025059.4:c.1892G>C MANE Select NP_079335.2:p.Ser631Thr
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