Canonical Allele Identifier: CA1969296943
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235252G= , CM000673.2:g.47235252G= GRCh38
NC_000011.9:g.47256803G= , CM000673.1:g.47256803G= GRCh37
NC_000011.8:g.47213379G= NCBI36
NG_009365.1:g.25311G= , LRG_467:g.25311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000256996.9:c.881-18G= MANE Select ENSP00000256996.4:n.881-18G=
ENST00000256996.8:c.881-18G= ENSP00000256996.3:n.881-18G=
ENST00000378600.7:c.457-2585G= ENSP00000367863.3:n.457-2585G=
ENST00000378601.7:c.703-18G= ENSP00000367864.3:n.703-18G=
ENST00000378603.7:c.689-18G= ENSP00000367866.3:n.689-18G=
ENST00000612309.4:n.2312G=
ENST00000614394.1:n.271-18G=
ENST00000616278.4:c.557-18G= ENSP00000478411.1:n.557-18G=
ENST00000617022.4:n.1554-2585G=
ENST00000617847.4:c.810-18G=
ENST00000620515.1:n.47-18G=
NM_000107.2:c.881-18G= , LRG_467t1:c.881-18G= NP_000098.1:n.881-18G=
NM_001300734.1:c.457-2585G= NP_001287663.1:n.457-2585G=
XR_242780.3:n.871-18G=
XR_242780.4:n.871-18G=
NM_000107.3:c.881-18G= MANE Select NP_000098.1:n.881-18G=
NM_001300734.2:c.457-2585G= NP_001287663.1:n.457-2585G=
NM_001399874.1:c.881-18G= NP_001386803.1:n.881-18G=
NM_001399875.1:c.881-18G= NP_001386804.1:n.881-18G=
NM_001399876.1:c.457-2585G= NP_001386805.1:n.457-2585G=
NM_001399878.1:c.689-18G= NP_001386807.1:n.689-18G=
NR_174610.1:n.1132-18G=
NR_174611.1:n.1110-18G=