Canonical Allele Identifier: CA16497353
Gene: RIN3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10498635

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.92636964C>T , CM000676.2:g.92636964C>T GRCh38
NC_000014.7:g.92173062C>T NCBI36
NC_000014.8:g.93103309C>T , CM000676.1:g.93103309C>T GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000216487.11:c.441-4274C>T ENSP00000216487.7:p.=
ENST00000418924.6:n.340-4274C>T
ENST00000554888.1:n.8-4274C>T
ENST00000555589.5:c.368-4274C>T ENSP00000450682.1:p.=
ENST00000620541.4:c.441-4274C>T ENSP00000480603.1:p.=
NM_024832.3:c.441-4274C>T VV NP_079108.3:p.=
XM_011537163.1:c.216-4274C>T XP_011535465.1:p.=
XM_011537164.1:c.213-4274C>T XP_011535466.1:p.=
XM_011537165.1:c.-571-4274C>T XP_011535467.1:p.=
NM_001319987.1:c.216-4274C>T VV NP_001306916.1:p.=
NM_024832.4:c.441-4274C>T VV
XM_011537164.3:c.213-4274C>T
XM_011537165.3:c.-571-4274C>T
XM_017021651.2:c.348-4274C>T XP_016877140.1:p.=
XM_017021652.1:c.441-4274C>T XP_016877141.1:p.=
XM_017021653.1:c.441-4274C>T XP_016877142.1:p.=
XM_017021654.1:c.441-4274C>T XP_016877143.1:p.=