Canonical Allele Identifier: CA363281146
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1759382055
gnomAD v4: 6-24301835-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301835T>C , CM000668.2:g.24301835T>C GRCh38
NC_000006.11:g.24302063T>C , CM000668.1:g.24302063T>C GRCh37
NC_000006.10:g.24410042T>C NCBI36
NG_012829.1:g.61218A>G
NG_012829.2:g.86458A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.437A>G MANE Select ENSP00000367715.3:p.Asn146Ser
ENST00000378454.7:c.437A>G ENSP00000367715.3:p.Asn146Ser
NM_001195610.1:c.437A>G NP_001182539.1:p.Asn146Ser
NM_016356.4:c.437A>G NP_057440.2:p.Asn146Ser
NM_016356.5:c.437A>G MANE Select NP_057440.2:p.Asn146Ser
NM_001195610.2:c.437A>G NP_001182539.1:p.Asn146Ser