Canonical Allele Identifier: CA1914338228
Gene: ARID5B HGNC NCBI

Linked Data

dbSNP Id: rs1838870236

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.61988024C>T , CM000672.2:g.61988024C>T GRCh38
NC_000010.10:g.63747783C>T , CM000672.1:g.63747783C>T GRCh37
NC_000010.9:g.63417789C>T NCBI36
NG_030027.1:g.91771C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000279873.12:c.503-12067C>T MANE Select ENSP00000279873.7:n.503-12067C>T
ENST00000644638.1:c.503-12067C>T ENSP00000494412.1:n.503-12067C>T
ENST00000681100.1:c.503-12067C>T ENSP00000506119.1:n.503-12067C>T
ENST00000279873.11:c.503-12067C>T ENSP00000279873.7:n.503-12067C>T
NM_032199.2:c.503-12067C>T NP_115575.1:n.503-12067C>T
XM_011540262.1:c.502+47616C>T XP_011538564.1:n.502+47616C>T
XM_024448230.1:c.-65-12067C>T XP_024303998.1:n.-65-12067C>T
NM_032199.3:c.503-12067C>T MANE Select NP_115575.1:n.503-12067C>T