Canonical Allele Identifier: CA667224986

Gene: ARID5B

Linked Data

• dbSNP Id: rs1203525477
• MyVariant Identifiers: chr10:g.63752020C>A (hg19) ; chr10:g.61992261C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992261C>A , CM000672.2:g.61992261C>A	GRCh38
NC_000010.10:g.63752020C>A , CM000672.1:g.63752020C>A	GRCh37
NC_000010.9:g.63422026C>A	NCBI36
NG_030027.1:g.96008C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-7830C>A MANE Select	ENSP00000279873.7:n.503-7830C>A
ENST00000644638.1:c.503-7830C>A	ENSP00000494412.1:n.503-7830C>A
ENST00000681100.1:c.503-7830C>A	ENSP00000506119.1:n.503-7830C>A
ENST00000279873.11:c.503-7830C>A	ENSP00000279873.7:n.503-7830C>A
NM_032199.2:c.503-7830C>A	NP_115575.1:n.503-7830C>A
XM_011540262.1:c.502+51853C>A	XP_011538564.1:n.502+51853C>A
XM_024448230.1:c.-65-7830C>A	XP_024303998.1:n.-65-7830C>A
NM_032199.3:c.503-7830C>A MANE Select	NP_115575.1:n.503-7830C>A