Canonical Allele Identifier: CA2711122736
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs138297758
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204634A>G , CM000668.2:g.24204634A>G GRCh38
NC_000006.11:g.24204862A>G , CM000668.1:g.24204862A>G GRCh37
NC_000006.10:g.24312841A>G NCBI36
NG_012829.1:g.158419T>C
NG_012829.2:g.183659T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+368T>C MANE Select ENSP00000367715.3:n.1023+368T>C
ENST00000378450.6:c.282+368T>C ENSP00000367711.3:n.282+368T>C
ENST00000378454.7:c.1023+368T>C ENSP00000367715.3:n.1023+368T>C
NM_001195610.1:c.1023+368T>C NP_001182539.1:n.1023+368T>C
NM_016356.4:c.1023+368T>C NP_057440.2:n.1023+368T>C
NM_016356.5:c.1023+368T>C MANE Select NP_057440.2:n.1023+368T>C
NM_001195610.2:c.1023+368T>C NP_001182539.1:n.1023+368T>C
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