Canonical Allele Identifier: CA11293414
Gene: DIS3L2 HGNC NCBI

Linked Data

dbSNP Id: rs7571816

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232212354A>G , CM000664.2:g.232212354A>G GRCh38
NC_000002.11:g.233077064A>G , CM000664.1:g.233077064A>G GRCh37
NC_000002.10:g.232785308A>G NCBI36
NG_032572.1:g.255772A>G , LRG_534:g.255772A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000325385.12:c.1204+1949A>G MANE Select ENSP00000315569.7:n.1204+1949A>G
ENST00000273009.10:c.1204+1949A>G ENSP00000273009.6:n.1204+1949A>G
ENST00000325385.11:c.1204+1949A>G ENSP00000315569.7:n.1204+1949A>G
ENST00000390005.9:c.1204+1949A>G ENSP00000374655.5:n.1204+1949A>G
ENST00000409307.5:c.1204+1949A>G ENSP00000386799.1:n.1204+1949A>G
ENST00000424049.1:c.109+1949A>G ENSP00000415419.1:n.109+1949A>G
ENST00000433430.5:c.1513+1949A>G ENSP00000391175.1:n.1513+1949A>G
ENST00000445090.5:c.*430+1949A>G ENSP00000388999.1:n.*430+1949A>G
NM_001257281.1:c.1204+1949A>G NP_001244210.1:n.1204+1949A>G
NM_152383.4:c.1204+1949A>G , LRG_534t1:c.1204+1949A>G NP_689596.4:n.1204+1949A>G
NR_046476.1:n.1480+1949A>G
NR_046477.1:n.1456+1949A>G
NM_001257281.2:c.1204+1949A>G NP_001244210.1:n.1204+1949A>G
NM_152383.5:c.1204+1949A>G MANE Select NP_689596.4:n.1204+1949A>G
NR_046476.2:n.1350+1949A>G
NR_046477.2:n.1326+1949A>G