Canonical Allele Identifier: CA136642195
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs532991585
gnomAD v3: 6-24347830-G-C
gnomAD v4: 6-24347830-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347830G>C , CM000668.2:g.24347830G>C GRCh38
NC_000006.11:g.24348058G>C , CM000668.1:g.24348058G>C GRCh37
NC_000006.10:g.24456037G>C NCBI36
NG_012829.1:g.15223C>G
NG_012829.2:g.40463C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5739C>G MANE Select ENSP00000367715.3:n.348+5739C>G
ENST00000378454.7:c.348+5739C>G ENSP00000367715.3:n.348+5739C>G
NM_001195610.1:c.348+5739C>G NP_001182539.1:n.348+5739C>G
NM_016356.4:c.348+5739C>G NP_057440.2:n.348+5739C>G
NM_016356.5:c.348+5739C>G MANE Select NP_057440.2:n.348+5739C>G
NM_001195610.2:c.348+5739C>G NP_001182539.1:n.348+5739C>G