Canonical Allele Identifier: CA2711321023
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs2127252584

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347981T>C , CM000668.2:g.24347981T>C GRCh38
NC_000006.11:g.24348209T>C , CM000668.1:g.24348209T>C GRCh37
NC_000006.10:g.24456188T>C NCBI36
NG_012829.1:g.15072A>G
NG_012829.2:g.40312A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5588A>G MANE Select ENSP00000367715.3:n.348+5588A>G
ENST00000378454.7:c.348+5588A>G ENSP00000367715.3:n.348+5588A>G
NM_001195610.1:c.348+5588A>G NP_001182539.1:n.348+5588A>G
NM_016356.4:c.348+5588A>G NP_057440.2:n.348+5588A>G
NM_016356.5:c.348+5588A>G MANE Select NP_057440.2:n.348+5588A>G
NM_001195610.2:c.348+5588A>G NP_001182539.1:n.348+5588A>G