Canonical Allele Identifier: CA929189986

Gene: JMJD1C

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.63373396A>T , CM000672.2:g.63373396A>T	GRCh38
NC_000010.10:g.65133156A>T , CM000672.1:g.65133156A>T	GRCh37
NC_000010.9:g.64803162A>T	NCBI36
NG_053187.1:g.153680T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399262.7:c.333+6922T>A MANE Select	ENSP00000382204.2:n.333+6922T>A
ENST00000399262.6:c.333+6922T>A	ENSP00000382204.2:n.333+6922T>A
ENST00000633035.1:n.278+6922T>A
NM_032776.2:c.333+6922T>A	NP_116165.1:n.333+6922T>A
XM_011539502.1:c.-214+6922T>A	XP_011537804.1:n.-214+6922T>A
XM_011539503.1:c.-214+6922T>A	XP_011537805.1:n.-214+6922T>A
XM_011539504.1:c.-214+6922T>A	XP_011537806.1:n.-214+6922T>A
XM_011539507.1:c.-214+6922T>A	XP_011537809.1:n.-214+6922T>A
XM_011539508.1:c.-214+6922T>A	XP_011537810.1:n.-214+6922T>A
XR_945628.1:n.165+6922T>A
XR_945629.1:n.165+6922T>A
NM_001318154.1:c.-214+6922T>A	NP_001305083.1:n.-214+6922T>A
NM_001322252.1:c.333+6922T>A	NP_001309181.1:n.333+6922T>A
NM_001322258.1:c.-219+6922T>A	NP_001309187.1:n.-219+6922T>A
XM_011539508.2:c.-214+6922T>A	XP_011537810.1:n.-214+6922T>A
XM_017015897.1:c.-100+6922T>A	XP_016871386.1:n.-100+6922T>A
XM_017015898.1:c.-214+6922T>A	XP_016871387.1:n.-214+6922T>A
XM_017015899.1:c.-536+6922T>A	XP_016871388.1:n.-536+6922T>A
XM_017015900.1:c.-536+6922T>A	XP_016871389.1:n.-536+6922T>A
XM_017015901.1:c.-430+6922T>A	XP_016871390.1:n.-430+6922T>A
XM_017015902.1:c.-430+6922T>A	XP_016871391.1:n.-430+6922T>A
XM_017015903.1:c.-316+6922T>A	XP_016871392.1:n.-316+6922T>A
XM_024447882.1:c.-219+6922T>A	XP_024303650.1:n.-219+6922T>A
XM_024447883.1:c.-105+6922T>A	XP_024303651.1:n.-105+6922T>A
NM_032776.3:c.333+6922T>A MANE Select	NP_116165.1:n.333+6922T>A
NM_001318154.2:c.-214+6922T>A	NP_001305083.1:n.-214+6922T>A
NM_001322252.2:c.333+6922T>A	NP_001309181.1:n.333+6922T>A
NM_001322258.2:c.-219+6922T>A	NP_001309187.1:n.-219+6922T>A