Canonical Allele Identifier: CA136625877

Gene: DCDC2

Linked Data

• dbSNP Id: rs970220525
• MyVariant Identifiers: chr6:g.24207136C>T (hg19) ; chr6:g.24206908C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206908C>T , CM000668.2:g.24206908C>T	GRCh38
NC_000006.11:g.24207136C>T , CM000668.1:g.24207136C>T	GRCh37
NC_000006.10:g.24315115C>T	NCBI36
NG_012829.1:g.156145G>A
NG_012829.2:g.181385G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.923-1806G>A MANE Select	ENSP00000367715.3:n.923-1806G>A
ENST00000378454.7:c.923-1806G>A	ENSP00000367715.3:n.923-1806G>A
NM_001195610.1:c.923-1806G>A	NP_001182539.1:n.923-1806G>A
NM_016356.4:c.923-1806G>A	NP_057440.2:n.923-1806G>A
NM_016356.5:c.923-1806G>A MANE Select	NP_057440.2:n.923-1806G>A
NM_001195610.2:c.923-1806G>A	NP_001182539.1:n.923-1806G>A