Canonical Allele Identifier: CA474228394

Gene: DDB2

Linked Data

• MyVariant Identifiers: chr11:g.47256349G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234798G>C , CM000673.2:g.47234798G>C	GRCh38
NC_000011.9:g.47256349G>C , CM000673.1:g.47256349G>C	GRCh37
NC_000011.8:g.47212925G>C	NCBI36
NG_009365.1:g.24857G>C , LRG_467:g.24857G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.744G>C MANE Select	ENSP00000256996.4:p.Val248=
ENST00000256996.8:c.744G>C	ENSP00000256996.3:p.Val248=
ENST00000378600.7:c.457-3039G>C	ENSP00000367863.3:n.457-3039G>C
ENST00000378601.7:c.702+126G>C	ENSP00000367864.3:n.702+126G>C
ENST00000378603.7:c.552G>C	ENSP00000367866.3:p.Val184=
ENST00000612309.4:n.1858G>C
ENST00000614394.1:n.134G>C
ENST00000616278.4:c.556+126G>C	ENSP00000478411.1:n.556+126G>C
ENST00000617022.4:n.1554-3039G>C
ENST00000617847.4:c.673G>C
ENST00000620515.1:n.46+126G>C
NM_000107.2:c.744G>C , LRG_467t1:c.744G>C	NP_000098.1:p.Val248=
NM_001300734.1:c.457-3039G>C	NP_001287663.1:n.457-3039G>C
XR_242780.3:n.870+126G>C
XR_242780.4:n.870+126G>C
NM_000107.3:c.744G>C MANE Select	NP_000098.1:p.Val248=
NM_001300734.2:c.457-3039G>C	NP_001287663.1:n.457-3039G>C
NM_001399874.1:c.744G>C	NP_001386803.1:p.Val248=
NM_001399875.1:c.744G>C	NP_001386804.1:p.Val248=
NM_001399876.1:c.457-3039G>C	NP_001386805.1:n.457-3039G>C
NM_001399878.1:c.552G>C	NP_001386807.1:p.Val184=
NR_174610.1:n.1131+126G>C
NR_174611.1:n.1031G>C