Canonical Allele Identifier: CA929073650
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838840800
gnomAD v3: 10-61985905-T-C
gnomAD v4: 10-61985905-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61985905T>C , CM000672.2:g.61985905T>C GRCh38
NC_000010.10:g.63745664T>C , CM000672.1:g.63745664T>C GRCh37
NC_000010.9:g.63415670T>C NCBI36
NG_030027.1:g.89652T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-14186T>C MANE Select ENSP00000279873.7:n.503-14186T>C
ENST00000644638.1:c.503-14186T>C ENSP00000494412.1:n.503-14186T>C
ENST00000681100.1:c.503-14186T>C ENSP00000506119.1:n.503-14186T>C
ENST00000279873.11:c.503-14186T>C ENSP00000279873.7:n.503-14186T>C
NM_032199.2:c.503-14186T>C NP_115575.1:n.503-14186T>C
XM_011540262.1:c.502+45497T>C XP_011538564.1:n.502+45497T>C
XM_024448230.1:c.-65-14186T>C XP_024303998.1:n.-65-14186T>C
NM_032199.3:c.503-14186T>C MANE Select NP_115575.1:n.503-14186T>C
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