Canonical Allele Identifier: CA208543994
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs994347259
gnomAD v3: 10-61963656-A-C
gnomAD v4: 10-61963656-A-C
MyVariant Identifiers: chr10:g.63723415A>C (hg19) chr10:g.61963656A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61963656A>C , CM000672.2:g.61963656A>C GRCh38
NC_000010.10:g.63723415A>C , CM000672.1:g.63723415A>C GRCh37
NC_000010.9:g.63393421A>C NCBI36
NG_030027.1:g.67403A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000279873.12:c.502+23248A>C MANE Select ENSP00000279873.7:n.502+23248A>C
ENST00000644638.1:c.502+23248A>C ENSP00000494412.1:n.502+23248A>C
ENST00000681100.1:c.502+23248A>C ENSP00000506119.1:n.502+23248A>C
ENST00000279873.11:c.502+23248A>C ENSP00000279873.7:n.502+23248A>C
NM_032199.2:c.502+23248A>C NP_115575.1:n.502+23248A>C
XM_011540262.1:c.502+23248A>C XP_011538564.1:n.502+23248A>C
XM_024448230.1:c.-66+23248A>C XP_024303998.1:n.-66+23248A>C
NM_032199.3:c.502+23248A>C MANE Select NP_115575.1:n.502+23248A>C
Search 100 bp 5'
Search 100 bp 3'