Canonical Allele Identifier: CA1616321947
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1581566482

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174728T>G , CM000668.2:g.24174728T>G GRCh38
NC_000006.11:g.24174956T>G , CM000668.1:g.24174956T>G GRCh37
NC_000006.10:g.24282935T>G NCBI36
NG_012829.1:g.188325A>C
NG_012829.2:g.213565A>C

Transcript Alleles

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