Canonical Allele Identifier: CA2500335016

Gene: JARID2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15267851C>A , CM000668.2:g.15267851C>A	GRCh38
NC_000006.11:g.15268082C>A , CM000668.1:g.15268082C>A	GRCh37
NC_000006.10:g.15376061C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341776.7:c.45+21267C>A MANE Select	ENSP00000341280.2:n.45+21267C>A
ENST00000341776.6:c.45+21267C>A	ENSP00000341280.2:n.45+21267C>A
ENST00000397311.4:c.-472+18887C>A	ENSP00000380478.3:n.-472+18887C>A
NM_001267040.1:c.-472+18887C>A	NP_001253969.1:n.-472+18887C>A
NM_004973.3:c.45+21267C>A	NP_004964.2:n.45+21267C>A
XM_005249089.2:c.-330+18887C>A	XP_005249146.1:n.-330+18887C>A
XM_011514578.1:c.-517+18887C>A	XP_011512880.1:n.-517+18887C>A
XM_011514579.1:c.45+21267C>A	XP_011512881.1:n.45+21267C>A
XM_011514580.1:c.45+21267C>A	XP_011512882.1:n.45+21267C>A
XM_011514582.1:c.-194+21267C>A	XP_011512884.1:n.-194+21267C>A
XM_011514579.3:c.45+21267C>A	XP_011512881.1:n.45+21267C>A
XM_017010833.2:c.45+21267C>A	XP_016866322.1:n.45+21267C>A
XM_017010834.2:c.-330+21267C>A	XP_016866323.1:n.-330+21267C>A
NM_004973.4:c.45+21267C>A MANE Select	NP_004964.2:n.45+21267C>A