Canonical Allele Identifier: CA566215157

Gene: DCDC2

Linked Data

• dbSNP Id: rs928980665
• gnomAD v2: 6-24207172-G-C
• gnomAD v3: 6-24206944-G-C
• gnomAD v4: 6-24206944-G-C
• MyVariant Identifiers: chr6:g.24207172G>C (hg19) ; chr6:g.24206944G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24206944G>C , CM000668.2:g.24206944G>C	GRCh38
NC_000006.11:g.24207172G>C , CM000668.1:g.24207172G>C	GRCh37
NC_000006.10:g.24315151G>C	NCBI36
NG_012829.1:g.156109C>G
NG_012829.2:g.181349C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378454.8:c.923-1842C>G MANE Select	ENSP00000367715.3:n.923-1842C>G
ENST00000378454.7:c.923-1842C>G	ENSP00000367715.3:n.923-1842C>G
NM_001195610.1:c.923-1842C>G	NP_001182539.1:n.923-1842C>G
NM_016356.4:c.923-1842C>G	NP_057440.2:n.923-1842C>G
NM_016356.5:c.923-1842C>G MANE Select	NP_057440.2:n.923-1842C>G
NM_001195610.2:c.923-1842C>G	NP_001182539.1:n.923-1842C>G