Canonical Allele Identifier: CA136636009
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs766481219
gnomAD v4: 6-24290803-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290803T>C , CM000668.2:g.24290803T>C GRCh38
NC_000006.11:g.24291031T>C , CM000668.1:g.24291031T>C GRCh37
NC_000006.10:g.24399010T>C NCBI36
NG_012829.1:g.72250A>G
NG_012829.2:g.97490A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+129A>G MANE Select ENSP00000367715.3:n.704+129A>G
ENST00000378454.7:c.704+129A>G ENSP00000367715.3:n.704+129A>G
NM_001195610.1:c.704+129A>G NP_001182539.1:n.704+129A>G
NM_016356.4:c.704+129A>G NP_057440.2:n.704+129A>G
NM_016356.5:c.704+129A>G MANE Select NP_057440.2:n.704+129A>G
NM_001195610.2:c.704+129A>G NP_001182539.1:n.704+129A>G