Canonical Allele Identifier: CA136637788
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1004219457
gnomAD v2: 6-24306386-G-A
gnomAD v3: 6-24306158-G-A
gnomAD v4: 6-24306158-G-A
MyVariant Identifiers: chr6:g.24306386G>A (hg19) chr6:g.24306158G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24306158G>A , CM000668.2:g.24306158G>A GRCh38
NC_000006.11:g.24306386G>A , CM000668.1:g.24306386G>A GRCh37
NC_000006.10:g.24414365G>A NCBI36
NG_012829.1:g.56895C>T
NG_012829.2:g.82135C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.349-4114C>T MANE Select ENSP00000367715.3:n.349-4114C>T
ENST00000378454.7:c.349-4114C>T ENSP00000367715.3:n.349-4114C>T
NM_001195610.1:c.349-4114C>T NP_001182539.1:n.349-4114C>T
NM_016356.4:c.349-4114C>T NP_057440.2:n.349-4114C>T
NM_016356.5:c.349-4114C>T MANE Select NP_057440.2:n.349-4114C>T
NM_001195610.2:c.349-4114C>T NP_001182539.1:n.349-4114C>T
Search 100 bp 5'
Search 100 bp 3'