Canonical Allele Identifier: CA2735262681
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs2144958308
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52665942A>C , CM000680.2:g.52665942A>C GRCh38
NC_000018.9:g.50192312A>C , CM000680.1:g.50192312A>C GRCh37
NC_000018.8:g.48446310A>C NCBI36
NG_013341.1:g.330771A>C
NG_013341.2:g.330771A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.92-86112A>C MANE Select ENSP00000389140.2:n.92-86112A>C
ENST00000442544.6:c.92-86112A>C ENSP00000389140.2:n.92-86112A>C
NM_005215.3:c.92-86112A>C NP_005206.2:n.92-86112A>C
XM_011525843.1:c.92-86112A>C XP_011524145.1:n.92-86112A>C
XM_011525845.1:c.92-86112A>C XP_011524147.1:n.92-86112A>C
XM_011525846.1:c.92-86112A>C XP_011524148.1:n.92-86112A>C
XM_017025568.1:c.92-86112A>C XP_016881057.1:n.92-86112A>C
XM_017025569.1:c.92-86112A>C XP_016881058.1:n.92-86112A>C
NM_005215.4:c.92-86112A>C MANE Select NP_005206.2:n.92-86112A>C
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