Canonical Allele Identifier: CA1835868612
Gene: CCDC171 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15986718T= , CM000671.2:g.15986718T= GRCh38
NC_000009.11:g.15986716T= , CM000671.1:g.15986716T= GRCh37
NC_000009.10:g.15976716T= NCBI36
NG_052634.1:g.438845T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000486641.2:n.369-33871T=
XM_017014432.2:c.3870-31585T= XP_016869921.1:n.3870-31585T=
XM_017014437.2:c.3778-35614T= XP_016869926.1:n.3778-35614T=
XR_001746227.2:n.4248-49375T=
XR_001746228.2:n.4248-35614T=