Canonical Allele Identifier: CA594062377
Gene: JMJD1C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.63361805C>T , CM000672.2:g.63361805C>T GRCh38
NC_000010.10:g.65121565C>T , CM000672.1:g.65121565C>T GRCh37
NC_000010.9:g.64791571C>T NCBI36
NG_053187.1:g.165271G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399262.7:c.333+18513G>A MANE Select ENSP00000382204.2:n.333+18513G>A
ENST00000399262.6:c.333+18513G>A ENSP00000382204.2:n.333+18513G>A
ENST00000633035.1:n.278+18513G>A
NM_032776.2:c.333+18513G>A NP_116165.1:n.333+18513G>A
XM_011539502.1:c.-214+18513G>A XP_011537804.1:n.-214+18513G>A
XM_011539503.1:c.-214+18513G>A XP_011537805.1:n.-214+18513G>A
XM_011539504.1:c.-214+18513G>A XP_011537806.1:n.-214+18513G>A
XM_011539507.1:c.-214+18513G>A XP_011537809.1:n.-214+18513G>A
XM_011539508.1:c.-214+18513G>A XP_011537810.1:n.-214+18513G>A
XR_945628.1:n.165+18513G>A
XR_945629.1:n.165+18513G>A
NM_001318154.1:c.-214+18513G>A NP_001305083.1:n.-214+18513G>A
NM_001322252.1:c.333+18513G>A NP_001309181.1:n.333+18513G>A
NM_001322258.1:c.-219+18513G>A NP_001309187.1:n.-219+18513G>A
XM_011539508.2:c.-214+18513G>A XP_011537810.1:n.-214+18513G>A
XM_017015897.1:c.-100+18513G>A XP_016871386.1:n.-100+18513G>A
XM_017015898.1:c.-214+18513G>A XP_016871387.1:n.-214+18513G>A
XM_017015899.1:c.-536+18513G>A XP_016871388.1:n.-536+18513G>A
XM_017015900.1:c.-536+18513G>A XP_016871389.1:n.-536+18513G>A
XM_017015901.1:c.-430+18513G>A XP_016871390.1:n.-430+18513G>A
XM_017015902.1:c.-430+18513G>A XP_016871391.1:n.-430+18513G>A
XM_017015903.1:c.-316+18513G>A XP_016871392.1:n.-316+18513G>A
XM_024447882.1:c.-219+18513G>A XP_024303650.1:n.-219+18513G>A
XM_024447883.1:c.-105+18513G>A XP_024303651.1:n.-105+18513G>A
NM_032776.3:c.333+18513G>A MANE Select NP_116165.1:n.333+18513G>A
NM_001318154.2:c.-214+18513G>A NP_001305083.1:n.-214+18513G>A
NM_001322252.2:c.333+18513G>A NP_001309181.1:n.333+18513G>A
NM_001322258.2:c.-219+18513G>A NP_001309187.1:n.-219+18513G>A
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