Canonical Allele Identifier: CA208313134

Gene: ARID5B

Linked Data

• dbSNP Id: rs761780076
• gnomAD v2: 10-63751932-GTC-G
• gnomAD v3: 10-61992173-GTC-G
• gnomAD v4: 10-61992173-GTC-G
• MyVariant Identifiers: chr10:g.63751933_63751934del (hg19) ; chr10:g.61992174_61992175del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992176_61992177del , CM000672.2:g.61992176_61992177del	GRCh38
NC_000010.10:g.63751935_63751936del , CM000672.1:g.63751935_63751936del	GRCh37
NC_000010.9:g.63421941_63421942del	NCBI36
NG_030027.1:g.95923_95924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-7915_503-7914del MANE Select	ENSP00000279873.7:n.503-7915_503-7914del
ENST00000644638.1:c.503-7915_503-7914del	ENSP00000494412.1:n.503-7915_503-7914del
ENST00000681100.1:c.503-7915_503-7914del	ENSP00000506119.1:n.503-7915_503-7914del
ENST00000279873.11:c.503-7915_503-7914del	ENSP00000279873.7:n.503-7915_503-7914del
NM_032199.2:c.503-7915_503-7914del	NP_115575.1:n.503-7915_503-7914del
XM_011540262.1:c.502+51768_502+51769del	XP_011538564.1:n.502+51768_502+51769del
XM_024448230.1:c.-65-7915_-65-7914del	XP_024303998.1:n.-65-7915_-65-7914del
NM_032199.3:c.503-7915_503-7914del MANE Select	NP_115575.1:n.503-7915_503-7914del