Canonical Allele Identifier: CA820885208

Gene: JARID2

Linked Data

• dbSNP Id: rs1165041225
• gnomAD v3: 6-15267822-C-A
• gnomAD v4: 6-15267822-C-A
• MyVariant Identifiers: chr6:g.15268053C>A (hg19) ; chr6:g.15267822C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15267822C>A , CM000668.2:g.15267822C>A	GRCh38
NC_000006.11:g.15268053C>A , CM000668.1:g.15268053C>A	GRCh37
NC_000006.10:g.15376032C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341776.7:c.45+21238C>A MANE Select	ENSP00000341280.2:n.45+21238C>A
ENST00000341776.6:c.45+21238C>A	ENSP00000341280.2:n.45+21238C>A
ENST00000397311.4:c.-472+18858C>A	ENSP00000380478.3:n.-472+18858C>A
NM_001267040.1:c.-472+18858C>A	NP_001253969.1:n.-472+18858C>A
NM_004973.3:c.45+21238C>A	NP_004964.2:n.45+21238C>A
XM_005249089.2:c.-330+18858C>A	XP_005249146.1:n.-330+18858C>A
XM_011514578.1:c.-517+18858C>A	XP_011512880.1:n.-517+18858C>A
XM_011514579.1:c.45+21238C>A	XP_011512881.1:n.45+21238C>A
XM_011514580.1:c.45+21238C>A	XP_011512882.1:n.45+21238C>A
XM_011514582.1:c.-194+21238C>A	XP_011512884.1:n.-194+21238C>A
XM_011514579.3:c.45+21238C>A	XP_011512881.1:n.45+21238C>A
XM_017010833.2:c.45+21238C>A	XP_016866322.1:n.45+21238C>A
XM_017010834.2:c.-330+21238C>A	XP_016866323.1:n.-330+21238C>A
NM_004973.4:c.45+21238C>A MANE Select	NP_004964.2:n.45+21238C>A