Canonical Allele Identifier: CA208377993
Gene: JMJD1C HGNC NCBI

Linked Data

dbSNP Id: rs10995485

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.63267098G>C , CM000672.2:g.63267098G>C GRCh38
NC_000010.10:g.65026858G>C , CM000672.1:g.65026858G>C GRCh37
NC_000010.9:g.64696864G>C NCBI36
NG_053187.1:g.259978C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399262.7:c.334-2334C>G MANE Select ENSP00000382204.2:n.334-2334C>G
ENST00000399262.6:c.334-2334C>G ENSP00000382204.2:n.334-2334C>G
ENST00000402544.5:n.525+1565C>G
ENST00000469152.5:n.213+1565C>G
ENST00000489372.4:n.591+1565C>G
ENST00000542921.5:c.-214+1565C>G ENSP00000444682.1:n.-214+1565C>G
ENST00000633035.1:n.279-2334C>G
NM_001282948.1:c.-214+1565C>G NP_001269877.1:n.-214+1565C>G
NM_032776.2:c.334-2334C>G NP_116165.1:n.334-2334C>G
XM_005269624.2:c.-219+1565C>G XP_005269681.1:n.-219+1565C>G
XM_005269626.2:c.-536+1565C>G XP_005269683.1:n.-536+1565C>G
XM_011539502.1:c.-213-2334C>G XP_011537804.1:n.-213-2334C>G
XM_011539503.1:c.-213-2334C>G XP_011537805.1:n.-213-2334C>G
XM_011539504.1:c.-213-2334C>G XP_011537806.1:n.-213-2334C>G
XM_011539505.1:c.-105+1565C>G XP_011537807.1:n.-105+1565C>G
XM_011539506.1:c.-347+1565C>G XP_011537808.1:n.-347+1565C>G
XM_011539507.1:c.-213-2334C>G XP_011537809.1:n.-213-2334C>G
XM_011539508.1:c.-213-2334C>G XP_011537810.1:n.-213-2334C>G
XR_945628.1:n.166-2334C>G
XR_945629.1:n.166-2334C>G
NM_001318153.1:c.-536+1565C>G NP_001305082.1:n.-536+1565C>G
NM_001318154.1:c.-213-2334C>G NP_001305083.1:n.-213-2334C>G
NM_001322252.1:c.334-47115C>G NP_001309181.1:n.334-47115C>G
NM_001322254.1:c.-219+1565C>G NP_001309183.1:n.-219+1565C>G
NM_001322258.1:c.-218-2334C>G NP_001309187.1:n.-218-2334C>G
NR_134512.1:n.561+1565C>G
XM_011539508.2:c.-213-2334C>G XP_011537810.1:n.-213-2334C>G
XM_017015897.1:c.-99-47115C>G XP_016871386.1:n.-99-47115C>G
XM_017015898.1:c.-213-2334C>G XP_016871387.1:n.-213-2334C>G
XM_017015899.1:c.-535-2334C>G XP_016871388.1:n.-535-2334C>G
XM_017015900.1:c.-535-2334C>G XP_016871389.1:n.-535-2334C>G
XM_017015901.1:c.-429-2334C>G XP_016871390.1:n.-429-2334C>G
XM_017015902.1:c.-429-2334C>G XP_016871391.1:n.-429-2334C>G
XM_017015903.1:c.-315-49767C>G XP_016871392.1:n.-315-49767C>G
XM_024447882.1:c.-218-2334C>G XP_024303650.1:n.-218-2334C>G
XM_024447883.1:c.-104-49767C>G XP_024303651.1:n.-104-49767C>G
NM_032776.3:c.334-2334C>G MANE Select NP_116165.1:n.334-2334C>G
NM_001318153.2:c.-536+1565C>G NP_001305082.1:n.-536+1565C>G
NM_001318154.2:c.-213-2334C>G NP_001305083.1:n.-213-2334C>G
NM_001322252.2:c.334-47115C>G NP_001309181.1:n.334-47115C>G
NM_001322254.2:c.-219+1565C>G NP_001309183.1:n.-219+1565C>G
NM_001322258.2:c.-218-2334C>G NP_001309187.1:n.-218-2334C>G
NM_001282948.2:c.-214+1565C>G NP_001269877.1:n.-214+1565C>G
NR_134512.2:n.581+1565C>G