Canonical Allele Identifier: CA3654765
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs535502253
gnomAD v2: 6-24302121-C-G
gnomAD v3: 6-24301893-C-G
gnomAD v4: 6-24301893-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301893C>G , CM000668.2:g.24301893C>G GRCh38
NC_000006.11:g.24302121C>G , CM000668.1:g.24302121C>G GRCh37
NC_000006.10:g.24410100C>G NCBI36
NG_012829.1:g.61160G>C
NG_012829.2:g.86400G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.426-47G>C MANE Select ENSP00000367715.3:n.426-47G>C
ENST00000378454.7:c.426-47G>C ENSP00000367715.3:n.426-47G>C
NM_001195610.1:c.426-47G>C NP_001182539.1:n.426-47G>C
NM_016356.4:c.426-47G>C NP_057440.2:n.426-47G>C
NM_016356.5:c.426-47G>C MANE Select NP_057440.2:n.426-47G>C
NM_001195610.2:c.426-47G>C NP_001182539.1:n.426-47G>C