Canonical Allele Identifier: CA1616446562
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1763726226
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290771A>G , CM000668.2:g.24290771A>G GRCh38
NC_000006.11:g.24290999A>G , CM000668.1:g.24290999A>G GRCh37
NC_000006.10:g.24398978A>G NCBI36
NG_012829.1:g.72282T>C
NG_012829.2:g.97522T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.704+161T>C MANE Select ENSP00000367715.3:n.704+161T>C
ENST00000378454.7:c.704+161T>C ENSP00000367715.3:n.704+161T>C
NM_001195610.1:c.704+161T>C NP_001182539.1:n.704+161T>C
NM_016356.4:c.704+161T>C NP_057440.2:n.704+161T>C
NM_016356.5:c.704+161T>C MANE Select NP_057440.2:n.704+161T>C
NM_001195610.2:c.704+161T>C NP_001182539.1:n.704+161T>C
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