Canonical Allele Identifier: CA136625871
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs955363182
gnomAD v3: 6-24206840-A-T
gnomAD v4: 6-24206840-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24206840A>T , CM000668.2:g.24206840A>T GRCh38
NC_000006.11:g.24207068A>T , CM000668.1:g.24207068A>T GRCh37
NC_000006.10:g.24315047A>T NCBI36
NG_012829.1:g.156213T>A
NG_012829.2:g.181453T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.923-1738T>A MANE Select ENSP00000367715.3:n.923-1738T>A
ENST00000378454.7:c.923-1738T>A ENSP00000367715.3:n.923-1738T>A
NM_001195610.1:c.923-1738T>A NP_001182539.1:n.923-1738T>A
NM_016356.4:c.923-1738T>A NP_057440.2:n.923-1738T>A
NM_016356.5:c.923-1738T>A MANE Select NP_057440.2:n.923-1738T>A
NM_001195610.2:c.923-1738T>A NP_001182539.1:n.923-1738T>A