Canonical Allele Identifier: CA1056965865
Gene: CCDC39 HGNC NCBI

Linked Data

dbSNP Id: rs1351662479
gnomAD v3: 3-180659596-C-G
gnomAD v4: 3-180659596-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.180659596C>G , CM000665.2:g.180659596C>G GRCh38
NC_000003.11:g.180377384C>G , CM000665.1:g.180377384C>G GRCh37
NC_000003.10:g.181860078C>G NCBI36
NG_029581.1:g.24900G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000476379.6:c.610-16G>C MANE Select ENSP00000417960.2:n.610-16G>C
ENST00000650641.1:n.689-16G>C
ENST00000650889.1:n.782-16G>C
ENST00000651046.1:c.610-16G>C ENSP00000499175.1:n.610-16G>C
ENST00000651818.1:n.752-16G>C
ENST00000652024.1:n.701-16G>C
ENST00000652408.1:n.747-16G>C
ENST00000442201.6:c.610-16G>C ENSP00000405708.2:n.610-16G>C
ENST00000476379.5:c.610-16G>C ENSP00000417960.1:n.610-16G>C
NM_181426.1:c.610-16G>C NP_852091.1:n.610-16G>C
NM_181426.2:c.610-16G>C MANE Select NP_852091.1:n.610-16G>C
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