Canonical Allele Identifier: CA208659425
Gene: JMJD1C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.63374062A>G , CM000672.2:g.63374062A>G GRCh38
NC_000010.10:g.65133822A>G , CM000672.1:g.65133822A>G GRCh37
NC_000010.9:g.64803828A>G NCBI36
NG_053187.1:g.153014T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399262.7:c.333+6256T>C MANE Select ENSP00000382204.2:n.333+6256T>C
ENST00000399262.6:c.333+6256T>C ENSP00000382204.2:n.333+6256T>C
ENST00000633035.1:n.278+6256T>C
NM_032776.2:c.333+6256T>C NP_116165.1:n.333+6256T>C
XM_011539502.1:c.-214+6256T>C XP_011537804.1:n.-214+6256T>C
XM_011539503.1:c.-214+6256T>C XP_011537805.1:n.-214+6256T>C
XM_011539504.1:c.-214+6256T>C XP_011537806.1:n.-214+6256T>C
XM_011539507.1:c.-214+6256T>C XP_011537809.1:n.-214+6256T>C
XM_011539508.1:c.-214+6256T>C XP_011537810.1:n.-214+6256T>C
XR_945628.1:n.165+6256T>C
XR_945629.1:n.165+6256T>C
NM_001318154.1:c.-214+6256T>C NP_001305083.1:n.-214+6256T>C
NM_001322252.1:c.333+6256T>C NP_001309181.1:n.333+6256T>C
NM_001322258.1:c.-219+6256T>C NP_001309187.1:n.-219+6256T>C
XM_011539508.2:c.-214+6256T>C XP_011537810.1:n.-214+6256T>C
XM_017015897.1:c.-100+6256T>C XP_016871386.1:n.-100+6256T>C
XM_017015898.1:c.-214+6256T>C XP_016871387.1:n.-214+6256T>C
XM_017015899.1:c.-536+6256T>C XP_016871388.1:n.-536+6256T>C
XM_017015900.1:c.-536+6256T>C XP_016871389.1:n.-536+6256T>C
XM_017015901.1:c.-430+6256T>C XP_016871390.1:n.-430+6256T>C
XM_017015902.1:c.-430+6256T>C XP_016871391.1:n.-430+6256T>C
XM_017015903.1:c.-316+6256T>C XP_016871392.1:n.-316+6256T>C
XM_024447882.1:c.-219+6256T>C XP_024303650.1:n.-219+6256T>C
XM_024447883.1:c.-105+6256T>C XP_024303651.1:n.-105+6256T>C
NM_032776.3:c.333+6256T>C MANE Select NP_116165.1:n.333+6256T>C
NM_001318154.2:c.-214+6256T>C NP_001305083.1:n.-214+6256T>C
NM_001322252.2:c.333+6256T>C NP_001309181.1:n.333+6256T>C
NM_001322258.2:c.-219+6256T>C NP_001309187.1:n.-219+6256T>C
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