Canonical Allele Identifier: CA3654731
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs561849262
ExAC: 6:24301944 T / C
gnomAD v2: 6-24301944-T-C
gnomAD v3: 6-24301716-T-C
gnomAD v4: 6-24301716-T-C
MyVariant Identifiers: chr6:g.24301944T>C (hg19) chr6:g.24301716T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301716T>C , CM000668.2:g.24301716T>C GRCh38
NC_000006.11:g.24301944T>C , CM000668.1:g.24301944T>C GRCh37
NC_000006.10:g.24409923T>C NCBI36
NG_012829.1:g.61337A>G
NG_012829.2:g.86577A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.556A>G MANE Select ENSP00000367715.3:p.Arg186Gly
ENST00000378454.7:c.556A>G ENSP00000367715.3:p.Arg186Gly
NM_001195610.1:c.556A>G NP_001182539.1:p.Arg186Gly
NM_016356.4:c.556A>G NP_057440.2:p.Arg186Gly
NM_016356.5:c.556A>G MANE Select NP_057440.2:p.Arg186Gly
NM_001195610.2:c.556A>G NP_001182539.1:p.Arg186Gly
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