Canonical Allele Identifier: CA1616324774
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760957846
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177807A>G , CM000668.2:g.24177807A>G GRCh38
NC_000006.11:g.24178035A>G , CM000668.1:g.24178035A>G GRCh37
NC_000006.10:g.24286014A>G NCBI36
NG_012829.1:g.185246T>C
NG_012829.2:g.210486T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1326+523T>C MANE Select ENSP00000367715.3:n.1326+523T>C
ENST00000378450.6:c.585+523T>C ENSP00000367711.3:n.585+523T>C
ENST00000378454.7:c.1326+523T>C ENSP00000367715.3:n.1326+523T>C
NM_001195610.1:c.1326+523T>C NP_001182539.1:n.1326+523T>C
NM_016356.4:c.1326+523T>C NP_057440.2:n.1326+523T>C
NM_016356.5:c.1326+523T>C MANE Select NP_057440.2:n.1326+523T>C
NM_001195610.2:c.1326+523T>C NP_001182539.1:n.1326+523T>C
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