Canonical Allele Identifier: CA594066888

Gene: JMJD1C

Linked Data

• dbSNP Id: rs946858570
• gnomAD v2: 10-65274805-T-G
• gnomAD v3: 10-63515045-T-G
• gnomAD v4: 10-63515045-T-G
• MyVariant Identifiers: chr10:g.65274805T>G (hg19) ; chr10:g.63515045T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.63515045T>G , CM000672.2:g.63515045T>G	GRCh38
NC_000010.10:g.65274805T>G , CM000672.1:g.65274805T>G	GRCh37
NC_000010.9:g.64944811T>G	NCBI36
NG_053187.1:g.12031A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000633035.1:n.113+6693A>C
NM_001318154.1:c.-379+6693A>C	NP_001305083.1:n.-379+6693A>C
NM_001322258.1:c.-384+6693A>C	NP_001309187.1:n.-384+6693A>C
XM_017015897.1:c.-265+6693A>C	XP_016871386.1:n.-265+6693A>C
XM_017015899.1:c.-701+6693A>C	XP_016871388.1:n.-701+6693A>C
XM_017015901.1:c.-595+6693A>C	XP_016871390.1:n.-595+6693A>C
XM_017015903.1:c.-481+6693A>C	XP_016871392.1:n.-481+6693A>C
NM_001318154.2:c.-379+6693A>C	NP_001305083.1:n.-379+6693A>C
NM_001322258.2:c.-384+6693A>C	NP_001309187.1:n.-384+6693A>C