Canonical Allele Identifier: CA448951376
Gene: DCDC2 HGNC NCBI

Linked Data

gnomAD v4: 6-24301807-G-C
MyVariant Identifiers: chr6:g.24302035G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301807G>C , CM000668.2:g.24301807G>C GRCh38
NC_000006.11:g.24302035G>C , CM000668.1:g.24302035G>C GRCh37
NC_000006.10:g.24410014G>C NCBI36
NG_012829.1:g.61246C>G
NG_012829.2:g.86486C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.465C>G MANE Select ENSP00000367715.3:p.Arg155=
ENST00000378454.7:c.465C>G ENSP00000367715.3:p.Arg155=
NM_001195610.1:c.465C>G NP_001182539.1:p.Arg155=
NM_016356.4:c.465C>G NP_057440.2:p.Arg155=
NM_016356.5:c.465C>G MANE Select NP_057440.2:p.Arg155=
NM_001195610.2:c.465C>G NP_001182539.1:p.Arg155=