Canonical Allele Identifier: CA431779095
Gene: DIS3L2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.233198561C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232333851C>T , CM000664.2:g.232333851C>T GRCh38
NC_000002.11:g.233198561C>T , CM000664.1:g.233198561C>T GRCh37
NC_000002.10:g.232906805C>T NCBI36
NG_032572.1:g.377269C>T , LRG_534:g.377269C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000325385.12:c.2022C>T MANE Select ENSP00000315569.7:p.Tyr674=
ENST00000273009.10:c.1582-9494C>T ENSP00000273009.6:n.1582-9494C>T
ENST00000325385.11:c.2022C>T ENSP00000315569.7:p.Tyr674=
ENST00000390005.9:c.*89C>T ENSP00000374655.5:n.*89C>T
ENST00000409307.5:c.2022C>T ENSP00000386799.1:p.Tyr674=
ENST00000424049.1:c.927C>T ENSP00000415419.1:p.Tyr309=
ENST00000429283.2:n.1588C>T
ENST00000433430.5:c.3433C>T ENSP00000391175.1:n.3433C>T
ENST00000445090.5:c.*1178C>T ENSP00000388999.1:n.*1178C>T
NM_001257281.1:c.1582-9494C>T NP_001244210.1:n.1582-9494C>T
NM_152383.4:c.2022C>T , LRG_534t1:c.2022C>T NP_689596.4:p.Tyr674=
NR_046476.1:n.2225C>T
NR_046477.1:n.2204C>T
NM_001257281.2:c.1582-9494C>T NP_001244210.1:n.1582-9494C>T
NM_152383.5:c.2022C>T MANE Select NP_689596.4:p.Tyr674=
NR_046476.2:n.2095C>T
NR_046477.2:n.2074C>T