Canonical Allele Identifier: CA2721587055

Gene: ARID5B

Linked Data

• dbSNP Id: rs1450406969

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62019971G>A , CM000672.2:g.62019971G>A	GRCh38
NC_000010.10:g.63779730G>A , CM000672.1:g.63779730G>A	GRCh37
NC_000010.9:g.63449736G>A	NCBI36
NG_030027.1:g.123718G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.733+19650G>A MANE Select	ENSP00000279873.7:n.733+19650G>A
ENST00000644638.1:c.734-4702G>A	ENSP00000494412.1:n.734-4702G>A
ENST00000681100.1:c.733+19650G>A	ENSP00000506119.1:n.733+19650G>A
ENST00000279873.11:c.733+19650G>A	ENSP00000279873.7:n.733+19650G>A
NM_032199.2:c.733+19650G>A	NP_115575.1:n.733+19650G>A
XM_011540262.1:c.503-30917G>A	XP_011538564.1:n.503-30917G>A
XM_024448230.1:c.166+19650G>A	XP_024303998.1:n.166+19650G>A
NM_032199.3:c.733+19650G>A MANE Select	NP_115575.1:n.733+19650G>A