Canonical Allele Identifier: CA929073679
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838841258
gnomAD v3: 10-61985935-A-T
gnomAD v4: 10-61985935-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985935A>T , CM000672.2:g.61985935A>T GRCh38
NC_000010.10:g.63745694A>T , CM000672.1:g.63745694A>T GRCh37
NC_000010.9:g.63415700A>T NCBI36
NG_030027.1:g.89682A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-14156A>T MANE Select ENSP00000279873.7:n.503-14156A>T
ENST00000644638.1:c.503-14156A>T ENSP00000494412.1:n.503-14156A>T
ENST00000681100.1:c.503-14156A>T ENSP00000506119.1:n.503-14156A>T
ENST00000279873.11:c.503-14156A>T ENSP00000279873.7:n.503-14156A>T
NM_032199.2:c.503-14156A>T NP_115575.1:n.503-14156A>T
XM_011540262.1:c.502+45527A>T XP_011538564.1:n.502+45527A>T
XM_024448230.1:c.-65-14156A>T XP_024303998.1:n.-65-14156A>T
NM_032199.3:c.503-14156A>T MANE Select NP_115575.1:n.503-14156A>T
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