Canonical Allele Identifier: CA136642199
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs977262837
gnomAD v2: 6-24348065-G-GA
gnomAD v3: 6-24347837-G-GA
gnomAD v4: 6-24347837-G-GA
MyVariant Identifiers: chr6:g.24348065_24348066insA (hg19) chr6:g.24347837_24347838insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347844dup , CM000668.2:g.24347844dup GRCh38
NC_000006.11:g.24348072dup , CM000668.1:g.24348072dup GRCh37
NC_000006.10:g.24456051dup NCBI36
NG_012829.1:g.15215dup
NG_012829.2:g.40455dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5731dup MANE Select ENSP00000367715.3:n.348+5731dup
ENST00000378454.7:c.348+5731dup ENSP00000367715.3:n.348+5731dup
NM_001195610.1:c.348+5731dup NP_001182539.1:n.348+5731dup
NM_016356.4:c.348+5731dup NP_057440.2:n.348+5731dup
NM_016356.5:c.348+5731dup MANE Select NP_057440.2:n.348+5731dup
NM_001195610.2:c.348+5731dup NP_001182539.1:n.348+5731dup
Search 100 bp 5'
Search 100 bp 3'