Canonical Allele Identifier: CA823286299
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1462975222
MyVariant Identifiers: chr6:g.24178057T>G (hg19) chr6:g.24177829T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24177829T>G , CM000668.2:g.24177829T>G GRCh38
NC_000006.11:g.24178057T>G , CM000668.1:g.24178057T>G GRCh37
NC_000006.10:g.24286036T>G NCBI36
NG_012829.1:g.185224A>C
NG_012829.2:g.210464A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+501A>C MANE Select ENSP00000367715.3:n.1326+501A>C
ENST00000378450.6:c.585+501A>C ENSP00000367711.3:n.585+501A>C
ENST00000378454.7:c.1326+501A>C ENSP00000367715.3:n.1326+501A>C
NM_001195610.1:c.1326+501A>C NP_001182539.1:n.1326+501A>C
NM_016356.4:c.1326+501A>C NP_057440.2:n.1326+501A>C
NM_016356.5:c.1326+501A>C MANE Select NP_057440.2:n.1326+501A>C
NM_001195610.2:c.1326+501A>C NP_001182539.1:n.1326+501A>C
Search 100 bp 5'
Search 100 bp 3'