Canonical Allele Identifier: CA593888729

Gene: ARID5B

Linked Data

• dbSNP Id: rs1450406969
• gnomAD v2: 10-63779730-G-T
• gnomAD v3: 10-62019971-G-T
• gnomAD v4: 10-62019971-G-T
• MyVariant Identifiers: chr10:g.63779730G>T (hg19) ; chr10:g.62019971G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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