Canonical Allele Identifier: CA12408111
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs147064489

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206900T>G , CM000668.2:g.24206900T>G GRCh38
NC_000006.11:g.24207128T>G , CM000668.1:g.24207128T>G GRCh37
NC_000006.10:g.24315107T>G NCBI36
NG_012829.1:g.156153A>C
NG_012829.2:g.181393A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1798A>C MANE Select ENSP00000367715.3:n.923-1798A>C
ENST00000378454.7:c.923-1798A>C ENSP00000367715.3:n.923-1798A>C
NM_001195610.1:c.923-1798A>C NP_001182539.1:n.923-1798A>C
NM_016356.4:c.923-1798A>C NP_057440.2:n.923-1798A>C
NM_016356.5:c.923-1798A>C MANE Select NP_057440.2:n.923-1798A>C
NM_001195610.2:c.923-1798A>C NP_001182539.1:n.923-1798A>C