Canonical Allele Identifier: CA3654745
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs146953663
gnomAD v2: 6-24302036-C-T
gnomAD v3: 6-24301808-C-T
gnomAD v4: 6-24301808-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24301808C>T , CM000668.2:g.24301808C>T GRCh38
NC_000006.11:g.24302036C>T , CM000668.1:g.24302036C>T GRCh37
NC_000006.10:g.24410015C>T NCBI36
NG_012829.1:g.61245G>A
NG_012829.2:g.86485G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.464G>A MANE Select ENSP00000367715.3:p.Arg155His
ENST00000378454.7:c.464G>A ENSP00000367715.3:p.Arg155His
NM_001195610.1:c.464G>A NP_001182539.1:p.Arg155His
NM_016356.4:c.464G>A NP_057440.2:p.Arg155His
NM_016356.5:c.464G>A MANE Select NP_057440.2:p.Arg155His
NM_001195610.2:c.464G>A NP_001182539.1:p.Arg155His