Canonical Allele Identifier: CA136625862

Gene: DCDC2

Linked Data

• dbSNP Id: rs928950907
• MyVariant Identifiers: chr6:g.24206989G>T (hg19) ; chr6:g.24206761G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206761G>T , CM000668.2:g.24206761G>T	GRCh38
NC_000006.11:g.24206989G>T , CM000668.1:g.24206989G>T	GRCh37
NC_000006.10:g.24314968G>T	NCBI36
NG_012829.1:g.156292C>A
NG_012829.2:g.181532C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.923-1659C>A MANE Select	ENSP00000367715.3:n.923-1659C>A
ENST00000378454.7:c.923-1659C>A	ENSP00000367715.3:n.923-1659C>A
NM_001195610.1:c.923-1659C>A	NP_001182539.1:n.923-1659C>A
NM_016356.4:c.923-1659C>A	NP_057440.2:n.923-1659C>A
NM_016356.5:c.923-1659C>A MANE Select	NP_057440.2:n.923-1659C>A
NM_001195610.2:c.923-1659C>A	NP_001182539.1:n.923-1659C>A