Canonical Allele Identifier: CA4051986
Gene: CCDC170 HGNC NCBI

Linked Data

dbSNP Id: rs73617535
ExAC: 6:151936704 C / T
gnomAD v2: 6-151936704-C-T
gnomAD v3: 6-151615569-C-T
gnomAD v4: 6-151615569-C-T
MyVariant Identifiers: chr6:g.151936704C>T (hg19) chr6:g.151615569C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615569C>T , CM000668.2:g.151615569C>T GRCh38
NC_000006.11:g.151936704C>T , CM000668.1:g.151936704C>T GRCh37
NC_000006.10:g.151978397C>T NCBI36
NG_021198.1:g.126530C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1837C>T MANE Select ENSP00000239374.6:p.His613Tyr
ENST00000239374.7:c.1837C>T ENSP00000239374.6:p.His613Tyr
NM_025059.3:c.1837C>T NP_079335.2:p.His613Tyr
XM_011536147.1:c.1855C>T XP_011534449.1:p.His619Tyr
XM_011536148.1:c.1654C>T XP_011534450.1:p.His552Tyr
XM_011536147.2:c.1855C>T XP_011534449.1:p.His619Tyr
XM_011536148.2:c.1654C>T XP_011534450.1:p.His552Tyr
XR_001743865.1:n.129+1152G>A
NM_025059.4:c.1837C>T MANE Select NP_079335.2:p.His613Tyr
Search 100 bp 5'
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