Canonical Allele Identifier: CA820885209

Gene: JARID2

Linked Data

• dbSNP Id: rs1203333805
• MyVariant Identifiers: chr6:g.15268067_15268068del (hg19) ; chr6:g.15267836_15267837del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.15267839_15267840del , CM000668.2:g.15267839_15267840del	GRCh38
NC_000006.11:g.15268070_15268071del , CM000668.1:g.15268070_15268071del	GRCh37
NC_000006.10:g.15376049_15376050del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000341776.7:c.45+21255_45+21256del MANE Select	ENSP00000341280.2:n.45+21255_45+21256del
ENST00000341776.6:c.45+21255_45+21256del	ENSP00000341280.2:n.45+21255_45+21256del
ENST00000397311.4:c.-472+18875_-472+18876del	ENSP00000380478.3:n.-472+18875_-472+18876...
NM_001267040.1:c.-472+18875_-472+18876del	NP_001253969.1:n.-472+18875_-472+18876del...
NM_004973.3:c.45+21255_45+21256del	NP_004964.2:n.45+21255_45+21256del
XM_005249089.2:c.-330+18875_-330+18876del	XP_005249146.1:n.-330+18875_-330+18876del...
XM_011514578.1:c.-517+18875_-517+18876del	XP_011512880.1:n.-517+18875_-517+18876del...
XM_011514579.1:c.45+21255_45+21256del	XP_011512881.1:n.45+21255_45+21256del
XM_011514580.1:c.45+21255_45+21256del	XP_011512882.1:n.45+21255_45+21256del
XM_011514582.1:c.-194+21255_-194+21256del	XP_011512884.1:n.-194+21255_-194+21256del...
XM_011514579.3:c.45+21255_45+21256del	XP_011512881.1:n.45+21255_45+21256del
XM_017010833.2:c.45+21255_45+21256del	XP_016866322.1:n.45+21255_45+21256del
XM_017010834.2:c.-330+21255_-330+21256del	XP_016866323.1:n.-330+21255_-330+21256del...
NM_004973.4:c.45+21255_45+21256del MANE Select	NP_004964.2:n.45+21255_45+21256del