Canonical Allele Identifier: CA1616409061
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1320077109
gnomAD v4: 6-24301603-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301603G>C , CM000668.2:g.24301603G>C GRCh38
NC_000006.11:g.24301831G>C , CM000668.1:g.24301831G>C GRCh37
NC_000006.10:g.24409810G>C NCBI36
NG_012829.1:g.61450C>G
NG_012829.2:g.86690C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.557+112C>G MANE Select ENSP00000367715.3:n.557+112C>G
ENST00000378454.7:c.557+112C>G ENSP00000367715.3:n.557+112C>G
NM_001195610.1:c.557+112C>G NP_001182539.1:n.557+112C>G
NM_016356.4:c.557+112C>G NP_057440.2:n.557+112C>G
NM_016356.5:c.557+112C>G MANE Select NP_057440.2:n.557+112C>G
NM_001195610.2:c.557+112C>G NP_001182539.1:n.557+112C>G