Canonical Allele Identifier: CA136625661
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs920415704

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204779C>T , CM000668.2:g.24204779C>T GRCh38
NC_000006.11:g.24205007C>T , CM000668.1:g.24205007C>T GRCh37
NC_000006.10:g.24312986C>T NCBI36
NG_012829.1:g.158274G>A
NG_012829.2:g.183514G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+223G>A MANE Select ENSP00000367715.3:n.1023+223G>A
ENST00000378450.6:c.282+223G>A ENSP00000367711.3:n.282+223G>A
ENST00000378454.7:c.1023+223G>A ENSP00000367715.3:n.1023+223G>A
NM_001195610.1:c.1023+223G>A NP_001182539.1:n.1023+223G>A
NM_016356.4:c.1023+223G>A NP_057440.2:n.1023+223G>A
NM_016356.5:c.1023+223G>A MANE Select NP_057440.2:n.1023+223G>A
NM_001195610.2:c.1023+223G>A NP_001182539.1:n.1023+223G>A