Canonical Allele Identifier: CA667212051

Gene: ARID5B

Linked Data

• dbSNP Id: rs1349809112
• MyVariant Identifiers: chr10:g.63779816C>T (hg19) ; chr10:g.62020057C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.62020057C>T , CM000672.2:g.62020057C>T	GRCh38
NC_000010.10:g.63779816C>T , CM000672.1:g.63779816C>T	GRCh37
NC_000010.9:g.63449822C>T	NCBI36
NG_030027.1:g.123804C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000279873.12:c.733+19736C>T MANE Select	ENSP00000279873.7:n.733+19736C>T
ENST00000644638.1:c.734-4616C>T	ENSP00000494412.1:n.734-4616C>T
ENST00000681100.1:c.733+19736C>T	ENSP00000506119.1:n.733+19736C>T
ENST00000279873.11:c.733+19736C>T	ENSP00000279873.7:n.733+19736C>T
NM_032199.2:c.733+19736C>T	NP_115575.1:n.733+19736C>T
XM_011540262.1:c.503-30831C>T	XP_011538564.1:n.503-30831C>T
XM_024448230.1:c.166+19736C>T	XP_024303998.1:n.166+19736C>T
NM_032199.3:c.733+19736C>T MANE Select	NP_115575.1:n.733+19736C>T