Canonical Allele Identifier: CA2677515107
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24290834-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290834A>C , CM000668.2:g.24290834A>C GRCh38
NC_000006.11:g.24291062A>C , CM000668.1:g.24291062A>C GRCh37
NC_000006.10:g.24399041A>C NCBI36
NG_012829.1:g.72219T>G
NG_012829.2:g.97459T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+98T>G MANE Select ENSP00000367715.3:n.704+98T>G
ENST00000378454.7:c.704+98T>G ENSP00000367715.3:n.704+98T>G
NM_001195610.1:c.704+98T>G NP_001182539.1:n.704+98T>G
NM_016356.4:c.704+98T>G NP_057440.2:n.704+98T>G
NM_016356.5:c.704+98T>G MANE Select NP_057440.2:n.704+98T>G
NM_001195610.2:c.704+98T>G NP_001182539.1:n.704+98T>G