Canonical Allele Identifier: CA3654427
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs758240952
ExAC: 6:24174946 T / C
gnomAD v2: 6-24174946-T-C
gnomAD v3: 6-24174718-T-C
gnomAD v4: 6-24174718-T-C
MyVariant Identifiers: chr6:g.24174946T>C (hg19) chr6:g.24174718T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174718T>C , CM000668.2:g.24174718T>C GRCh38
NC_000006.11:g.24174946T>C , CM000668.1:g.24174946T>C GRCh37
NC_000006.10:g.24282925T>C NCBI36
NG_012829.1:g.188335A>G
NG_012829.2:g.213575A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*12A>G MANE Select ENSP00000367715.3:n.*12A>G
ENST00000378450.6:c.*12A>G ENSP00000367711.3:n.*12A>G
ENST00000378454.7:c.*12A>G ENSP00000367715.3:n.*12A>G
NM_001195610.1:c.*12A>G NP_001182539.1:n.*12A>G
NM_016356.4:c.*12A>G NP_057440.2:n.*12A>G
NM_016356.5:c.*12A>G MANE Select NP_057440.2:n.*12A>G
NM_001195610.2:c.*12A>G NP_001182539.1:n.*12A>G
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