Canonical Allele Identifier: CA823284543
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1442308634
MyVariant Identifiers: chr6:g.24278883T>G (hg19) chr6:g.24278655T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24278655T>G , CM000668.2:g.24278655T>G GRCh38
NC_000006.11:g.24278883T>G , CM000668.1:g.24278883T>G GRCh37
NC_000006.10:g.24386862T>G NCBI36
NG_012829.1:g.84398A>C
NG_012829.2:g.109638A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.760-444A>C MANE Select ENSP00000367715.3:n.760-444A>C
ENST00000378454.7:c.760-444A>C ENSP00000367715.3:n.760-444A>C
NM_001195610.1:c.760-444A>C NP_001182539.1:n.760-444A>C
NM_016356.4:c.760-444A>C NP_057440.2:n.760-444A>C
NM_016356.5:c.760-444A>C MANE Select NP_057440.2:n.760-444A>C
NM_001195610.2:c.760-444A>C NP_001182539.1:n.760-444A>C
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