Canonical Allele Identifier: CA136625888
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs793862

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206972A>G , CM000668.2:g.24206972A>G GRCh38
NC_000006.11:g.24207200A>G , CM000668.1:g.24207200A>G GRCh37
NC_000006.10:g.24315179A>G NCBI36
NG_012829.1:g.156081T>C
NG_012829.2:g.181321T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1870T>C MANE Select ENSP00000367715.3:n.923-1870T>C
ENST00000378454.7:c.923-1870T>C ENSP00000367715.3:n.923-1870T>C
NM_001195610.1:c.923-1870T>C NP_001182539.1:n.923-1870T>C
NM_016356.4:c.923-1870T>C NP_057440.2:n.923-1870T>C
NM_016356.5:c.923-1870T>C MANE Select NP_057440.2:n.923-1870T>C
NM_001195610.2:c.923-1870T>C NP_001182539.1:n.923-1870T>C