Canonical Allele Identifier: CA1616406103
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760294754

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347814A>T , CM000668.2:g.24347814A>T GRCh38
NC_000006.11:g.24348042A>T , CM000668.1:g.24348042A>T GRCh37
NC_000006.10:g.24456021A>T NCBI36
NG_012829.1:g.15239T>A
NG_012829.2:g.40479T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5755T>A MANE Select ENSP00000367715.3:n.348+5755T>A
ENST00000378454.7:c.348+5755T>A ENSP00000367715.3:n.348+5755T>A
NM_001195610.1:c.348+5755T>A NP_001182539.1:n.348+5755T>A
NM_016356.4:c.348+5755T>A NP_057440.2:n.348+5755T>A
NM_016356.5:c.348+5755T>A MANE Select NP_057440.2:n.348+5755T>A
NM_001195610.2:c.348+5755T>A NP_001182539.1:n.348+5755T>A